Substituted nitroaminophenols, process for their preparation and dyeing compositions in which they are present

Claim 2

A dye compound having the formula ##STR11## in which R 1 and R 2 are identical or different and represent hydrogen or alkyl having from 1 to 4 carbon atoms.

Claim 3

Dyeing composition for keratin fibres and human hair, which comprises, in aqueous solution, at least one dye compound of claim 1.

Claim 4

Composition of claim 2, which comprises from 0.002% to 5% by weight of at least one of said dye compounds.

Claim 5

Composition of claim 2 in which the pH of the composition is between 3 and 11.

Claim 6

Composition of claim 4, in which the pH is established by ammonia, organic amines or by sodium hydrogen phosphate.

Claim 7

Composition of claim 2 which can be used as a semi-permanent dye, that additionally contains nitro dyestuffs corresponding to the general formula: ##STR12## in which formula X represents hydrogen, halogen, alkyl, ##STR13## or OR 5 , with R 1 , R 2 , R 3 , R 4 and R 5 , which may be identical or different being hydrogen, alkyl or a substituted alkyl and Z represents hydrogen or halogen alkyl, alkoxy or NO 2 .

Claim 8

Composition of claim 2 which can be used in semi-permanent dyeing, which additionally contains anthraquinone dyestuffs, azo dyestuffs, oxazines, indoanilines or indophenols.

Claim 9

Composition of claim 2 which can be used as a colouring wavesetting lotion, that additionally contains, in aqueous-alcoholic solution, direct dyestuffs and at least one cosmetic resin.

Claim 10

Composition of claim 2, which can be used for obtaining permanent dyeings that additionally contains at least one oxidation dyestuff.

Claim 11

Composition of claim 9, that contains, as a mixture, at least one para-phenylenediamine or para-aminophenol oxidation base and at least one coupler.

Claim 12

Composition of claim 10, in which the oxidation base has the general formula ##STR14## in which R 1 , R, R 3 and R 4 are identical or different and represent hydrogen, alkyl, alkoxy or halogen, Z represents OH or ##STR15## R 5 and R 6 being identical or different and representing hydrogen, alkyl or substituted alkyl, with the reservation that R 1 and R 4 represent hydrogen when R 5 and R 6 do not represent hydrogen.

Claim 13

Composition of claim 10, in which the oxidation base contains a heterocyclic nucleus.

Claim 14

Composition of claim 10 in which the couplers are chosen from the group consisting of: (a) α-naphthol, resorcinol and its derivatives which are substituted in the nucleus, (b) the meta-aminophenols which are substituted in the nucleus or on the amine group and which correspond to the general formula ##STR16## in which R 1 and R 2 can be identical or different, and represent halogen, alkoxy, alkyl or hydrogen, Y represents hydrogen, alkoxy or alkyl, and Z represents alkyl, substituted alkyl, or acyl, ureido or carbethoxy group, with the reservation that R 2 must be hydrogen and Z must be hydrogen or alkyl or substituted alkyl when Y is an alkyl group, (c) the metadiamines, which can have substituents in the nucleus or on the amine group, (d) the couplers which comprise a pyridine nucleus and (e) the couplers of the group of pyrazolones, β-diketones and 6-hydroxy-phenomorpholine.

Claim 15

Composition of claim 2 that additionally contains at least one hair dyestuff which can undergo auto-oxidation.

Claim 16

Composition of claim 2 that additionally contains at least one product chosen from the group consisting of: (a) solvents other than water, (b) anionic, cationic or non-ionic surface-active agents, sulphonated esters of alcohol, sulphates of fatty alcohols and sodium lauryl sulphate, (c) thickening agents, (d) antioxydants, (e) sequestring agents and (f) perfumes.

Claim 17

Process of producing the compounds of claim 1, comprising reacting chloroethyl chloroformate with 3-nitro-4-amino-phenol, which is optionally substituted in the 2- and/or 6-position(s) by an alkyl radical having from 1 to 4 carbon atoms, the reaction taking place in dioxane in the presence of calcium carbonate, and in that an alkaline hydrolysis of the carbamate formed is carried out thereafter.

Claim 18

Process of claim 16, which the reaction with the chloroethyl chloroformate takes place at a temperature of between about 70 and 100° C.

Claim 19

Process of claim 16 in which the alkaline hydrolysis of the carbamate formed is carried out with a concentrated aqueous potassium hydroxide solution, at a temperature of between 0 and 25° C.

Claim 20

The compound of claim 1, which is 3-nitro-4-(β-hydroxyethylamino)-phenol.

Claim 21

The compound of claim 1, which is 2-methyl-4-(β-hydroxyethylamino)-5-nitro-phenol.

Claim 22

The compound of claim 1, which is 2,6-dimethyl-4-(β-hydroxyethylamino)-3-nitro-phenol.