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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27802Generated: October 26, 2026

Anisole → 4-Bromoanisole

https://huagongshe.com/reaction/27802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnisoleHCID 7519—
ReactantBromineHCID 24408—
SolventChloroformHCID 6212—
Product4-BromoanisoleHCID 773080%

Reaction Steps

The bromination of anisole with one equivalent of bromine is chloroform, at room temperature, is reported to give an 80% yield of monobromoanisole. Grignard, Bellet and Courtot, Ann. Chim. 4, 28 (1915). The preparation of dibromoanisole from anisole, and of tribromoanisole from dibromoanisole, in carbon tetrachloride, is also reported. Kohn and Sussman, Monatsh. Chem. 46, 575 (1925). "Several days" reaction time is reported for the preparation of several tribromophenyl alkyl ethers. Yields are not reported. Baiford and Birosel, J. Am. Chem. Soc., 51, 1776 (1929). The bromination of anisole with three equivalents of bromine yields 1.5% tribromoanisole. Similarly, the bromination of monobromoanisole with two equivalents of bromine in chloroform is reported to give only small quantities of tribromoanisole, and tribromoanisole is reported not to brominate further. D. M. Birosel, Univ. Phillipines Natural Applied Sci. Bull. 1, 145 (1931).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04223169
Source datasetuspto-grants-1980_09
ORD IDord-b3cef7a29b304f9cb7de60fa5db6d751
Source noteuspto-grants-1980_09