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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 920225생성일: 2026년 10월 26일

Chlorosulfonic acid → 5-Fluoro-2-oxo-2,3-dihydro-1,3-benzoxazole-6-sulfonyl chloride

https://huagongshe.com/reaction/920225

반응식

참여 물질

역할이름HCID투입량
반응물Chlorosulfonic acidHCID 24638—
반응물5-Fluoro-2(3H)-benzoxazoloneHCID 287208—
용매DichloromethaneHCID 6344—
생성물5-Fluoro-2-oxo-2,3-dihydro-1,3-benzoxazole-6-sulfonyl chlorideHCID 82276165—

반응 단계

According to Scheme 11, a mixture of commercially-available 5-fluoro-1,3-benzoxazol-2(3H)-one (11-1, 1.02 g, 6.66 mmol) in DCM (66.6 ml) at RT was added chlorosulfonic acid (4.46 ml, 66.6 mmol). The suspension gradually became a solution and was stirred for 18 h at RT. Following this duration, LCMS showed complete consumption of starting material. The solution was cooled to 0° C. and carefully quenched with ice chips and then partitioned between water (100 mL) and EtOAc (100 mL). The layers were separated and the aqueous layer was back-extracted with 3×20 mL DCM and 2×20 mL EtOAc. The combined organic layers were washed with saturated aqueous NaHCO3 (30 mL), dried over sodium sulfate and filtered. Concentration in vacuo to yield 11-2 (5-Fluoro-2-oxo-2,3-dihydro-1,3-benzoxazole-6-sulfonyl chloride) as a tan solid, which was used without purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09273040B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-272cfea00f6f45118157f9f20ec9a6d7
출처 메모uspto-grants-2016_03