GB347892A - Manufacture of aromatic condensation products - Google Patents

Manufacture of aromatic condensation products

Info

Publication number
GB347892A
GB347892A GB1403330A GB1403330A GB347892A GB 347892 A GB347892 A GB 347892A GB 1403330 A GB1403330 A GB 1403330A GB 1403330 A GB1403330 A GB 1403330A GB 347892 A GB347892 A GB 347892A
Authority
GB
United Kingdom
Prior art keywords
yields
derivative
chlormethyl
groups
halogenmethyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB1403330A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to GB1403330A priority Critical patent/GB347892A/en
Publication of GB347892A publication Critical patent/GB347892A/en
Expired legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Compounds containing halogenmethyl groups, in addition to alkoxy or alkylthio groups, are made by causing a benzene derivative which contains at least one alkoxy or alkylthio group, and either contains no further substituent, or contains as further substituent alkyl, halogen, or a nitrogroup, to react with formaldehyde in the presence of a concentrated hydrogen halide solution. According to the conditions of the reaction, either one or two halogenmethyl groups enter the molecule. In examples, by treating with an aqueous formaldehyde solution saturated with hydrochloric acid, (1) anisol yields 2 : 4-di(chlormethyl)-anisol, (2) m-chloranisol yields a mono-chlormethyl derivative, (3) p-cresolmethylether yields 3-chlormethyl-4-methoxytoluene, (4) hydroquinone-dimethylether yields the 2 : 5-dichlormethyl derivative (5) o-nitroanisol yields a mono-chlormethyl derivative, (6) p-thiocresolmethylether yields a monochlormethyl derivative, and (7) thiophenol-methylether yields the 2 : 4-di(chlormethyl) derivative. Specification 17118/99, [Class 2, Acids and salts, Organic &c.], is referred to.
GB1403330A 1930-05-07 1930-05-07 Manufacture of aromatic condensation products Expired GB347892A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1403330A GB347892A (en) 1930-05-07 1930-05-07 Manufacture of aromatic condensation products

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1403330A GB347892A (en) 1930-05-07 1930-05-07 Manufacture of aromatic condensation products

Publications (1)

Publication Number Publication Date
GB347892A true GB347892A (en) 1931-05-07

Family

ID=10033776

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1403330A Expired GB347892A (en) 1930-05-07 1930-05-07 Manufacture of aromatic condensation products

Country Status (1)

Country Link
GB (1) GB347892A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2695319A (en) * 1954-11-23 Process of producing verairyl

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2695319A (en) * 1954-11-23 Process of producing verairyl

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