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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1440736생성일: 2026년 10월 26일

Triethylamine → O-Isopropyl P-Ethyl[[(2,6-dichlorophenyl)sulfonyloxy]methyl]phosphinate

https://huagongshe.com/reaction/1440736

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2,6-DichlorobenzenesulfonylchlorideHCID 522183—
반응물O-isopropyl P-ethyl(hydroxymethyl)phosphinateHCID 15041111—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물O-Isopropyl P-Ethyl[[(2,6-dichlorophenyl)sulfonyloxy]methyl]phosphinateHCID 5417005865.4%

반응 단계

A solution of 19.6 g of 2,6-dichlorobenzenesulfonyl chloride dissolved in 70 ml of methylene chloride was added dropwise over 40 minutes to a mixture of 25 ml of methylene chloride, 15.0 ml of triethylamine, 1.0 g of DMAP, and 16.5 g of O-isopropyl P-ethyl(hydroxymethyl)phosphinate, (Example 22, Method A). The addition caused a mild exotherm and the reaction was allowed to stir at room temperature overnight. The reaction mixture was then washed with two 50 ml portions of water, the phases separated, the organic phase dried with magnesium sulfate, filtered, and concentrated to yield 19.6 g of the desired product as a yellow oil. The crude product was diluted with 10 ml of methylene chloride and flash chromatographed using blends of ethyl acetate and hexanes. Similar fractions were combined and rechromatographed to yield 0.95 g of the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05500405
출처 데이터셋uspto-grants-1996_03
ORD IDord-53d2d1166fd74845bbad8a9194b3be19
출처 메모uspto-grants-1996_03