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HRID 463898作成日:2026年10月26日

Dimethyl Sulfide → Dimethyl-2,6-difluorophenacylsulfonium bromide

https://huagongshe.com/reaction/463898

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfideHCID 1068—
反応物BromineHCID 24408—
反応物1-(2,6-Difluorophenyl)ethan-1-oneHCID 83643—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
生成物Dimethyl-2,6-difluorophenacylsulfonium bromideHCID 2026545138%

反応手順

A solution of bromine (4.1 ml, 80 mmoles) in dichloromethane (6 ml) was added dropwise to a solution of 2,6-difluoroacetophenone (12.4 g, 80 mmoles) in anhydrous diethyl ether (100 ml). The reaction solution was evaporated and the resulting liquid was dissolved in tetrahydrofuran (150 ml) and methyl sulfide (9 ml, 120 mmoles) was added. The mixture was allowed to stand at room temperature for 6 days (approximately 144 hours). The crystals were filtered to yield 8.9 g (38%) of dimethyl-2,6-difluorophenacylsulfonium bromide. A mixture of the sulfonium salt (8.9 g) and isopropyl nitrate (6.4 ml, 60 mmoles) was stirred in dichloromethane (80 ml) for 7 days (approximately 168 hours) at room temperature. The volatiles were evaporated and the residue was dissolved in diethyl ether (250 ml). The organic solution was washed 4 times with 100 ml portions of water, saturated sodium chloride, dried (sodium sulfate), and evaporated to give 6.8 g of a solid. Recrystallization from carbon tetrachloride (250 ml) gave 4.9 g (23%) of crystals, melting point 138°-140° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04544753
出典データセットuspto-grants-1985_10
ORD IDord-2aaa0e8df56e4065ba11a7362bf3e362
出典メモuspto-grants-1985_10