戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1464673作成日:2026年10月26日

Bromine → 3-Bromo-5-(p-chlorophenyl)-4-[(trifluoromethyl)sulfonyl]-2-[(trifluoromethyl)thio]pyrrole

https://huagongshe.com/reaction/1464673

反応式

関与物質

役割名称HCID仕込み量
反応物BromineHCID 24408—
反応物2-(p-Chlorophenyl)-3-[(trifluoromethyl)sulfonyl]-5-[(trifluoromethyl)thio]pyrroleHCID 18930406—
触媒BromineHCID 24408—
溶媒ChloroformHCID 6212—
溶媒DichloromethaneHCID 6344—
生成物3-Bromo-5-(p-chlorophenyl)-4-[(trifluoromethyl)sulfonyl]-2-[(trifluoromethyl)thio]pyrroleHCID 1893039041.9%

反応手順

A solution of 2-(p-chlorophenyl)-3-[(trifluoromethyl)sulfonyl]-5-[(trifluoromethyl)thio]pyrrole (0.5 g, 0.00122 mol) in chloroform (10 mL) is cooled with an ice bath, treated with a solution of bromine (0.21 g, 0.00134 mol) in chloroform (5 mL), stirred for two hours, warmed to room temperature, treated with two drops of additional bromine and stirred for one hour. The reaction mixture is diluted with methylene chloride, washed with water, saturated sodium hydrogen carbonate solution, saturated sodium metabisulfite solution and brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to obtain a syrup. Flash chromatography of the syrup using silica gel and a 1:5 ethyl acetate/hexanes solution gives the title product as a white solid (0.25 g, mp 122°-125° C.) which is identified by 1HNMR and 13CNMR spectral analyses.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05306827
出典データセットuspto-grants-1994_04
ORD IDord-c24cdfa4d1f2413daed18bb5f6baad4f
出典メモuspto-grants-1994_04