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HRID 745995作成日:2026年10月26日

Epibromohydrin → 1-Bromo-3-(4'-tert-butylphenylthio)-propan-2-ol

https://huagongshe.com/reaction/745995

反応式

関与物質

役割名称HCID仕込み量
反応物EpibromohydrinHCID 18430—
反応物4-Tert-ButylbenzenethiolHCID 75454—
反応物Triethylamine methanolHCID 22728368—
溶媒Diethyl EtherHCID 3283—
生成物1-Bromo-3-(4'-tert-butylphenylthio)-propan-2-olHCID 2331130492.7%

反応手順

To a stirred solution of 75.3 g [46.7 ml (0.55 mole)] 1-bromo-2,3-epoxypropane (epibromohydrin) in 14 ml 1:1 methanol/triethylamine cooled to 0°-5° C. in an ice-water bath, 83 g (0.5 mole) p-tert-butyl-thiophenol was added dropwise. After the addition was complete, the reaction mixture was allowed to come to room temperature and was stirred at room temperature for about 2 hours. The reaction mixture was dissolved in ethyl ether; washed with 1N sodium hydroxide, with 2N hydrochloric acid, with water until neutral and then with brine (twice). The organic phase was dried, filtered and concentrated to give 140.6 g of the above-identified product as an orange-red oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04602030
出典データセットuspto-grants-1986_07
ORD IDord-51507bba8cc441238c9b44c7248546b8
出典メモuspto-grants-1986_07