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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 509556생성일: 2026년 10월 24일

3-Oxo-azetidine-1-carboxylic acid tert-butyl ester → tert-Butyl 3-[(2-methylpropane-2-sulfinyl)imino]azetidine-1-carboxylate

https://huagongshe.com/ko/reaction/509556

반응식

참여 물질

역할이름HCID투입량
반응물3-Oxo-azetidine-1-carboxylic acid tert-butyl esterHCID 1519404—
반응물Tert-ButanesulfinamideHCID 3382465—
촉매HCID 178477244HCID 178477244—
용매TetrahydrofuranHCID 8028—
생성물tert-Butyl 3-[(2-methylpropane-2-sulfinyl)imino]azetidine-1-carboxylateHCID 5677698824%

반응 조건

온도70 °C

반응 단계

A mixture of tert-butyl 3-oxoazetidine-1-carboxylate (4 g, 23.37 mmol), 2-methylpropane-2-sulfinamide (3.12 g, 25.7 mmol) and tetraethoxytitanium (10.66 g, 46.7 mmol) in THF (40 ml) in a 20 ml sealed tube was stirred at 70° C. overnight. The reaction mixture was cooled to room temperature, quenched with water and filtered through a bed of Celite. The solid material was washed with ethyl acetate. The organic layer was separated, dried over Na2SO4, filtered and concentrated to obtain a crude mixture. The crude product was then purified by column chromatography (20% EtOAc in Hexane) to afford tert-butyl 3-(tert-butylsulfinylimino)azetidine-1-carboxylate Yield: 1.5 g (24%). 1H NMR (400 MHz, CDCl3): δ 5.15-4.94 (m, 1H), 4.75 (m, 1H), 4.68 (s, 2H), 1.45 (s, 9H), 1.27 (s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09096580B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-6457cae56dca409d9ce5a0a4b87ae24c
출처 메모uspto-grants-2015_08