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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 82962생성일: 2026년 10월 25일

Water → 1-(Diphenylmethyl)-3-(pentylsulfonyl)azetidine

https://huagongshe.com/reaction/82962

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sulfuric AcidHCID 1118—
반응물Sodium BicarbonateHCID 516892—
반응물Potassium hydroxy sulfiteHCID 23707502—
반응물1-(Diphenylmethyl)-3-(pentylthio)azetidineHCID 67154644—
용매MethanolHCID 887—
생성물1-(Diphenylmethyl)-3-(pentylsulfonyl)azetidineHCID 6715459430%

반응 단계

To a solution of 1-(diphenylmethyl)-3-(pentylthio)azetidine (228 mg, 0.70 mmol; which may be prepared as described in Step 2) in methanol (6.3 mL) and water (6.3 mL) was added H2SO4 1N (0.7 mL). The reaction mixture was stirred for 10 minutes, then oxone (1.08 g, 1.75 mmol) was added and the mixture stirred at room temperature for 12 h. A solution of saturated NaHCO3 (5 mL) was added and the mixture extracted with ethyl acetate. The two layers were separated and the organic washed with brine, dried over Na2SO4, filtered and concentrated. The crude was then purified on column chromatography (pentane/EtOAc, 100/0 then 90/10) to give the title product (75 mg, 30%) as a pale yellow oil. The less pure fraction (N-oxide) can be recycled in hydrogenolysis conditions.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846711B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-f630a1a4c82748fa9814874697e5c059
출처 메모uspto-grants-2014_09