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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6459생성일: 2026년 10월 23일

Water → (4R-cis)-1,1-dimethylethyl 6-(4-chlorobenzenesulfonyloxymethyl)-2,2-dimethyl-1,3-dioxane-4-acetate

https://huagongshe.com/ko/reaction/6459

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물4-Chlorobenzenesulfonyl chlorideHCID 7398—
반응물TriethylamineHCID 8471—
반응물tert-Butyl 2,4-dideoxy-3,5-O-(1-methylethylidene)-D-erythro-hexonateHCID 9816650—
용매DichloromethaneHCID 6344—
생성물(4R-cis)-1,1-dimethylethyl 6-(4-chlorobenzenesulfonyloxymethyl)-2,2-dimethyl-1,3-dioxane-4-acetateHCID 11797121130.1%

반응 단계

To a stirring, 0°-5° C. solution of the (4R-cis)-1,1-dimethylethyl 6-hydroxymethyl-2,2-dimethyl-1,3-dioxane-4-acetate (European Patent Application 0319,847) (10 g, 38 mmol) in methylene chloride (250 mL) containing triethylamine (10 mL, 72 mmol) is added 4-chlorobenzenesulfonyl chloride (12.7 g, 60 mmol). Stirring is continued at 0°-5° C. for 2.5 hours and the solution slowly warmed to 20°-25° C. over a period of 2 hours. The solution is poured onto 200 mL of water and the layers separated. The upper aqueous layer is extracted with 200 mL of methylene chloride and the combined organic layers are washed with 200 mL each of saturated sodium bicarbonate solution to ensure complete removal of 4-chlorobenzenesulfonyl chloride and then saturated sodium chloride solution. Drying the solution with magnesium sulfate and concentration in vacuo gives 21.5 g of the product as a pale yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05248793
출처 데이터셋uspto-grants-1993_09
ORD IDord-25c2d201df154c4a8596ac428de335f8
출처 메모uspto-grants-1993_09