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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-Oxo-azetidine-1-carboxylic acid tert-butyl ester | HCID 1519404 | — |
| 반응물 | Tert-Butanesulfinamide | HCID 3382465 | — |
| 촉매 | HCID 178477244 | HCID 178477244 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | tert-Butyl 3-[(2-methylpropane-2-sulfinyl)imino]azetidine-1-carboxylate | HCID 56776988 | 24% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09096580B2 |
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| 출처 데이터셋 | uspto-grants-2015_08 |
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| ORD ID | ord-6457cae56dca409d9ce5a0a4b87ae24c |
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| 출처 메모 | uspto-grants-2015_08 |
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