Process for preparing thiophene derivatives and thiophene derivatives obtained thereby

Claim 2

A process for the preparation of α-trihalomethyl-2-thiophenemethanols of the formula ##STR13## which comprises reacting a thiophene of the formula ##STR14## with a trihaloacetaldehyde of the formula CX 3 CHO under an acidic condition which is established by carrying out said reaction in the presence of an acid selected from the group consisting of (i) an ion-exchange resin comprising an acid supported on a polymer substance, (ii) titanium tetrachloride, and (iii) titanium tetrachloride and titanium tetraisopropoxide, at a temperature between 0° C. and the reflux temperature of the reaction mixture, wherein R 2 is hydrogen or a halogen atom; and X is selected from the group consisting of chlorine, bromine and iodine.

Claim 3

The process of claim 1, wherein said reaction is carried out in the presence of titanium tetrachloride.

Claim 4

The process of claim 1, wherein said reaction is carried out in the present of titanium tetrachloride and titanium tetraisopropoxide.

Claim 5

The process of claim 1, wherein said reaction is carried out in the presence of an ion-exchange resin comprising an acid supported on a polymer substance which is used to establish said acid condition.

Claim 6

The process of claim 1, wherein said α-trihalomethyl-2-thiophenemethanol product is separated from unreacted starting materials by utilizing the difference between their respective boiling points, and said unreacted starting materials are recycled to react under said acidic condition and said temperature.

Claim 7

The process of claim 1, wherein the molar ratio of said trihaloacetaldehyde to said thiophene is between about 1 and 2, and the molar ratio of said acid to said thiophene is not higher than 1.

Claim 8

A process for the preparation of α-substituted-2-thiopheneacetic acids of the formula ##STR15## which comprises reacting a thiophene of the formula ##STR16## with a trihaloacetaldehyde of the formula CX 3 CHO under an acidic condition which is established by carrying out said reaction in the presence of an acid selected from the group consisting of (i) an ion-exchange resin comprising an acid supported on a polymer substance, (ii) titanium tetrachloride, and (iii) titanium tetrachloride and titanium tetraisopropoxide, at a temperature between 0° C. and the reflux temperature of the reaction mixture, to form an α-trihalomethyl-2-thiophenemethanol of the formula ##STR17## and then reacting said α-trihalomethyl-2-thiphenemethanol with a compound of the formula R 3 H in the presence of a hydroxide selected from the group consisting of alkali and an alkaline earth metal hydroxides, at a temperature between room temperature and the reflux temperature of the reaction mixture, wherein R 2 is hydrogen or a halogen atom; R 3 is selected from the group consisting of alkoxyl groups, hydroxyl groups, alkylthio groups and arylthio groups; and X is selected from the group consisting of chlorine, bromine and iodine.

Claim 9

A process for the preparation of α-substituted-2-thiopheneacetic acids of the formula ##STR15## which comprises reacting a thiophene of the formula ##STR16## with a trihaloacetaldehyde of the formula CX 3 CHO under an acidic condition which is established by carrying out said reaction in the presence of an acid selected from the group consisting of (i) an ion-exchange resin comprising an acid supported on a polymer substance, (ii) titanium tetrachloride, and (iii) titanium tetrachloride and titanium tetraisopropoxide, at a temperature between 0° C. and the reflux temperature of the reaction mixture, to form an α-trihalomethyl-2-thiophenemethanol of the formula ##STR17## and then reacting said α-trihalomethyl-2-thiphenemethanol with a compound of the formula R 3 H in the presence of a hydroxide selected from the group consisting of alkali and an alkaline earth metal hydroxides, at a temperature between room temperature and the reflux temperature of the reaction mixture, wherein R 2 is hydrogen or a halogen atom; R 3 is selected from the group consisting of alkoxyl groups, hydroxyl groups, alkylthio groups and arylthio groups; and X is selected from the group consisting of chlorine, bromine and iodine.

Claim 10

The process of claim 7, wherein said hydroxide is sodium hydroxide or potassium hydroxide.

Claim 11

The process of claim 8, wherein 3 to 4 moles of said hydroxide are used per mole of said α-trihalomethyl-2-thiophenemethanol.

Claim 12

The process of claim 7, wherein an alcohol or an ether is present as a solvent.

Claim 13

The process of claim 7, wherein R 3 H is water.

Claim 14

The process of claim 7, wherein R 3 H is an alcohol.

Claim 15

The process of claim 7, wherein R 3 H is a thiol and 1 to 3 moles thiol are used per mole of said α-trihalomethyl-2-thiophenemethanol.

Claim 16

A process for the preparation of 2-thiopheneacetic acids of the formula ##STR18## which comprises reacting a thiophene of the formula ##STR19## with a trihaloacetaldehyde of the formula CX 3 CHO under an acidic condition which is established by carrying out said reaction in the presence of an acid selected from the group consisting of (i) an ion-exchange resin comprising an acid supported on a polymer substance, (ii) titanium tetrachloride, and (iii) titanium tetrachloride and titanium tetraisopropoxide, at a temperature between 0° C. and the reflux temperature of the reaction mixture, to form an α-trihalomethyl-2-thiophenemethanol of the formula ##STR20## and then reacting said α-trihalomethyl-2-thiophenemethanol with a compound of the formula R 3 H in the presence of an alkali or an alkaline earth metal hydroxide at a temperature between room temperature and the reflux temperature of the reaction mixture, to obtain an α-substituted 2-thiopheneacetic acid of the formula ##STR21## and then hydrogenating said α-substituted 2-thiopheneacetic acid by contacting with zinc and an acid, wherein R 2 is hydrogen or a halogen atom; R 3 is an alkylthio group or an arylthio group; and X is selected from the group consisting of chlorine, bromine and iodine.

Claim 17

A process for the preparation of 2-thiopheneacetic acids of the formula ##STR18## which comprises reacting a thiophene of the formula ##STR19## with a trihaloacetaldehyde of the formula CX 3 CHO under an acidic condition which is established by carrying out said reaction in the presence of an acid selected from the group consisting of (i) an ion-exchange resin comprising an acid supported on a polymer substance, (ii) titanium tetrachloride, and (iii) titanium tetrachloride and titanium tetraisopropoxide, at a temperature between 0° C. and the reflux temperature of the reaction mixture, to form an α-trihalomethyl-2-thiophenemethanol of the formula ##STR20## and then reacting said α-trihalomethyl-2-thiophenemethanol with a compound of the formula R 3 H in the presence of an alkali or an alkaline earth metal hydroxide at a temperature between room temperature and the reflux temperature of the reaction mixture, to obtain an α-substituted 2-thiopheneacetic acid of the formula ##STR21## and then hydrogenating said α-substituted 2-thiopheneacetic acid by contacting with zinc and an acid, wherein R 2 is hydrogen or a halogen atom; R 3 is an alkylthio group or an arylthio group; and X is selected from the group consisting of chlorine, bromine and iodine.

Claim 18

A process for the preparation of 2-thiopheneacetic acids of the formula ##STR22## which comprises reacting a thiophene of the formula ##STR23## with a trihaloacetaldehyde of the formula CX 3 CHO under an acidic condition which is established by carrying out said reaction in the presence of an acid selected from the group consisting of (i) an ion-exchange resin comprising an acid supported on a polymer substance, (ii) titanium tetrachloride, and (iii) titanium tetrachloride and titanium tetraisopropoxide, at a temperature between 0° C. and the reflux temperature of the reaction mixture, to form an α-trihalomethyl-2-thiophenemethanol of the formula ##STR24## and then reacting said α-trihalomethyl-2-thiophenemethanol with a compound of the general formula R 3 H in the presence of an alkali or an alkaline earth metal hydroxide at a temperature between room temperature and the reflux temperature of the reaction mixture to obtain an α-substituted 2-thiopheneacetic acid of the formula ##STR25## and then hydrogenating said α-substituted 2-thiopheneacetic acid by contacting with iodine and red phosphorus, wherein R 2 is hydrogen or a halogen atom; R 3 is an alkoxyl group or hydroxyl group; and X is selected from the group consisting of chlorine, bromine and iodine.

Claim 19

A process for the preparation of 2-thiopheneacetic acids of the formula ##STR22## which comprises reacting a thiophene of the formula ##STR23## with a trihaloacetaldehyde of the formula CX 3 CHO under an acidic condition which is established by carrying out said reaction in the presence of an acid selected from the group consisting of (i) an ion-exchange resin comprising an acid supported on a polymer substance, (ii) titanium tetrachloride, and (iii) titanium tetrachloride and titanium tetraisopropoxide, at a temperature between 0° C. and the reflux temperature of the reaction mixture, to form an α-trihalomethyl-2-thiophenemethanol of the formula ##STR24## and then reacting said α-trihalomethyl-2-thiophenemethanol with a compound of the general formula R 3 H in the presence of an alkali or an alkaline earth metal hydroxide at a temperature between room temperature and the reflux temperature of the reaction mixture to obtain an α-substituted 2-thiopheneacetic acid of the formula ##STR25## and then hydrogenating said α-substituted 2-thiopheneacetic acid by contacting with iodine and red phosphorus, wherein R 2 is hydrogen or a halogen atom; R 3 is an alkoxyl group or hydroxyl group; and X is selected from the group consisting of chlorine, bromine and iodine.