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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 893생성일: 2026년 10월 23일

Thionyl Chloride → (R)-4-methyl-3-(2-pyridyl)-[1,2,3]oxathiazolidine 2-oxide

https://huagongshe.com/ko/reaction/893

반응식

참여 물질

역할이름HCID투입량
반응물Thionyl ChlorideHCID 24386—
반응물DiisopropylethylamineHCID 81531—
반응물(R)-N-(2-pyridyl)-2-aminopropanolHCID 21339422—
용매DichloromethaneHCID 6344—
생성물(R)-4-methyl-3-(2-pyridyl)-[1,2,3]oxathiazolidine 2-oxideHCID 54573470599.1%

반응 단계

A solution of (R)-N-(2-pyridyl)-2-aminopropanol (20.0 g, 0.13 moles) and N,N-diisopropylethylamine (33.6 g, 0.13 moles) in dichloromethane (500 ml) was cooled to 5° C. Then thionyl chloride (15.5 g, 0.13 moles) in dichloromethane (100 ml) was added slowly whilst the temperature was kept below 10° C. The mixture was stirred for 0.5 h. and ice cold water (500 ml) was added. The organic phase was separated and washed with water (5×500 ml). The aqueous phase was back-extracted with dichloromethane (2×500 ml), the organic phases were combined, dried (MgSO4) and evaporated in vacuo to give a brown oil. This was purified on a silica column, eluting with diethyl ether to give (R)-4-methyl-3-(2-pyridyl)-[1,2,3] oxathiazolidine 2-oxide (154.4 g) as a clear oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723464
출처 데이터셋uspto-grants-1998_03
ORD IDord-696b27b131f24c17a8f31b09f5726b28
출처 메모uspto-grants-1998_03