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HRID 926030생성일: 2026년 10월 26일

Pyridine → 2-(Trimethylsilyl)ethyl 3-(chlorosulfonyl)benzoate

https://huagongshe.com/reaction/926030

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물DichloromethaneHCID 6344—
반응물2-(Trimethylsilyl)ethanolHCID 18013—
반응물Benzoyl chloride, 3-(chlorosulfonyl)-HCID 77671—
용매WaterHCID 962—
생성물2-(Trimethylsilyl)ethyl 3-(chlorosulfonyl)benzoateHCID 86676334—

반응 단계

To a mixture of 23.9 g of 3-(chlorosulfonyl)benzoyl chloride, 7.9 mL of pyridine, and 100 mL of dichloromethane was added dropwise 14 mL of 2-(trimethylsilyl)ethanol under ice-cooling, followed by stirring at room temperature for 2 hours. To the reaction mixture was added water, followed by extraction with chloroform, and the organic layer was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to obtain 29.4 g of 2-(trimethylsilyl)ethyl 3-(chlorosulfonyl)benzoate as a colorless solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09284295B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-fd932769b76a47e3ae3b4ecb47ed0316
출처 메모uspto-grants-2016_03