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HRID 27802作成日:2026年10月25日

Anisole → 4-Bromoanisole

https://huagongshe.com/reaction/27802

反応式

関与物質

役割名称HCID仕込み量
反応物AnisoleHCID 7519—
反応物BromineHCID 24408—
溶媒ChloroformHCID 6212—
生成物4-BromoanisoleHCID 773080%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04223169
出典データセットuspto-grants-1980_09
ORD IDord-b3cef7a29b304f9cb7de60fa5db6d751
出典メモuspto-grants-1980_09