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US3953510A Expired / Lapsed US ⏱️ 0.0 years remaining

Method for the preparation of alkoxyanilines

Assignee: Olin Corp
•
Filing: 1974-06-27
•
Granted: 1976-04-27
•
Expires: 1994-06-27
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Abstract

Abstract Alkoxyanilines are prepared in a one-step operation by reacting selected nitrobenzenes with selected alcohols and a deoxygenating agent in the presence of anhydrous hydrogen fluoride.

Inventors

  • 👤 Curtis P. Smith
  • 👤 Peter H. Scott

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-09 06:58
CPC Classifications
C; C07; C07C; C07C211/00; C07C211/43; C07C211/44; C07C211/52; C07C209/00; C07C209/04; C07C209/06; C07C209/10; C07C209/30; C07C209/32; C07C209/36; C07C211/54; C07C211/56; C07C213/00; C07C213/02

Claims Analysis

Total Claims: 14
Claim 1
Independent Claim 285 words
A method for preparing an o- or p- alkoxyaniline or substituted o- or p- alkoxyaniline which comprises reacting at a temperature of from about 20° to about 250°C. a mixture of a. a nitrobenzene selected from the group consisting of nitrobenzene and substituted nitrobenzene having as an additional substituent on the benzene ring at least one of the following: alkyl of 1 to 4 carbon atoms, halogen and nitro, with the proviso that at least one of the para or ortho positions to the nitro group is unsubstituted; b. an alcohol selected from the group consisting of unsubsituted, branched and unbranched, hydroxyalkyl and hydroxyalkenyl alcohols of 1 to 8 carbon atoms and polyoxyalkylene glycol ether alcohols of the formula: R(OR.sub.1).sub.x OH wherein R is an alkyl of 1 to 4 carbon atoms, R 1 is an ethylene or propylene group and x is 1 to 20; c. a deoxygenating agent selected from the group consisting of phosphorus, sulfur, phosphorus trihalides, sulfur halides in which sulfur has a valence lower than 6, aryl and diaryl phosphorus halides and aryl and diaryl sulfur halides, wherein the aryl group contains 6 to 10 carbon atoms, and triaryl phosphines wherein the aryl group contains 6 to 10 carbon atoms; and d. anhydrous hydrogen fluoride, said mixture containing a molar ratio of from about 1:1 to about 50:1 of said alcohol to said selected nitrobenzene, a molar ratio of from about 0.3:1 to about 5:1 of said deoxygenating agent to said selected nitrobenzene and a molar ratio of about 1:1 to about 50:1 of said hydrogen fluoride to said selected nitrobenzene and then separating said resulting o- or p- alkoxyaniline or o- or p- substituted alkoxyaniline from the reaction mixture.
Claim 2
Independent Claim 285 words
A method for preparing an o- or p- alkoxyaniline or substituted o- or p- alkoxyaniline which comprises reacting at a temperature of from about 20° to about 250°C. a mixture of a. a nitrobenzene selected from the group consisting of nitrobenzene and substituted nitrobenzene having as an additional substituent on the benzene ring at least one of the following: alkyl of 1 to 4 carbon atoms, halogen and nitro, with the proviso that at least one of the para or ortho positions to the nitro group is unsubstituted; b. an alcohol selected from the group consisting of unsubsituted, branched and unbranched, hydroxyalkyl and hydroxyalkenyl alcohols of 1 to 8 carbon atoms and polyoxyalkylene glycol ether alcohols of the formula: R(OR.sub.1).sub.x OH wherein R is an alkyl of 1 to 4 carbon atoms, R 1 is an ethylene or propylene group and x is 1 to 20; c. a deoxygenating agent selected from the group consisting of phosphorus, sulfur, phosphorus trihalides, sulfur halides in which sulfur has a valence lower than 6, aryl and diaryl phosphorus halides and aryl and diaryl sulfur halides, wherein the aryl group contains 6 to 10 carbon atoms, and triaryl phosphines wherein the aryl group contains 6 to 10 carbon atoms; and d. anhydrous hydrogen fluoride, said mixture containing a molar ratio of from about 1:1 to about 50:1 of said alcohol to said selected nitrobenzene, a molar ratio of from about 0.3:1 to about 5:1 of said deoxygenating agent to said selected nitrobenzene and a molar ratio of about 1:1 to about 50:1 of said hydrogen fluoride to said selected nitrobenzene and then separating said resulting o- or p- alkoxyaniline or o- or p- substituted alkoxyaniline from the reaction mixture.
Claim 3
Dependent Claim 12 words
The method of claim 1 wherein said deoxygenating agent is triphenyl phosphine.
Claim 4
Dependent Claim 21 words
The method of claim 1 wherein the molar ratio of alcohol to selected nitrobenzene is from about 2:1 to about 30:1.
Claim 5
Dependent Claim 22 words
The method of claim 1 wherein the molar ratio of hydrogen fluoride to selected nitrobenzene is from about 1:1 to about 30:1.
Claim 6
Dependent Claim 22 words
The method of claim 1 wherein the molar ratio of deoxygenating agent to selected nitrobenzene is from about 0.5:1 to about 2:1.
Claim 7
Dependent Claim 14 words
The method of claim 1 wherein nitrobenzene is reacted with ethanol to form p-ethoxyaniline.
Claim 8
Dependent Claim 14 words
The method of claim 1 wherein nitrobenzene is reacted with methanol to form p-methoxyaniline.
Claim 9
Dependent Claim 14 words
The method of claim 1 wherein nitrobenzene is reacted with propanol to form p-propoxyaniline.
Claim 10
Dependent Claim 15 words
The method of claim 1 wherein said temperature is from about 90° to about 165°C.
Claim 11
Dependent Claim 18 words
The method of claim 1 wherein said alcohol is an hydroxyalkyl alcohol of 1 to 8 carbon atoms.
Claim 12
Dependent Claim 63 words
The method of claim 1 wherein said mixture contains a molar ratio of from about 2:1 to about 30:1 of said alcohol to said selected nitrobenzene, a molar ratio of from about 0.5:1 to about 2:1 of said deoxygenating agent to said selected nitrobenzene and a molar ratio of from about 1:1 to about 30:1 of said hydrogen fluoride to said selected nitrobenzene.
Claim 13
Dependent Claim 29 words
The method of claim 1 wherein said alcohol is selected from the group consisting of unsubstituted, branched and unbranched, hydroxyalkyl and hydroxyalkenyl alcohols of 1 to 8 carbon atoms.
Claim 14
Dependent Claim 14 words
The method of claim 12 wherein said alcohol contains 1 to 4 carbon atoms.

References Cited (Backward Citations)

US3558707A Cited
US3580951A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1979-04-27 1979-10-27 1980-04-27 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1983-04-27 1983-10-27 1984-04-27 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1987-04-27 1987-10-27 1988-04-27 $7700.00 Window Closed / Lapsed

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