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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1039967생성일: 2026년 10월 25일

Ethyl diazoacetate → Ethyl 3-{[tert-butyl(dimethyl)silyl]oxy}bicyclo[3.1.0]hexane-6-carboxylate

https://huagongshe.com/reaction/1039967

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl diazoacetateHCID 12192—
반응물Tert-butyl(cyclopent-3-en-1-yloxy)dimethylsilaneHCID 11106335—
촉매Dirhodium tetraacetateHCID 152122—
생성물Ethyl 3-{[tert-butyl(dimethyl)silyl]oxy}bicyclo[3.1.0]hexane-6-carboxylateHCID 6743209173%

반응 단계

To a flask was added tert-butyl(cyclopent-3-en-1-yloxy)dimethylsilane (0.5 g, 2.52 mmol) and rhodium(II) acetate dimer (22 mg, 0.05 mmol). The flask was evacuated and purged 5 times with argon. Dichloromethane (8.4 mL) was added and the flask was evacuated and purged 5 times with argon. In a separate flask, ethyl diazoacetate (0.37 mL, 3.02 mmol) was added. The flask was evacuated and purged with argon five times. Dichloromethane (8.4 mL) was added and the solution was added to the first flask via syringe pump over a six hour time period and then allowed to stir overnight. The mixture was filtered over a pad of celite and then concentrated. Flash chromatography was used for purification to yield ethyl 3-{[tert-butyl(dimethyl)silyl]oxy}bicyclo[3.1.0]hexane-6-carboxylate (524 mg, 1.84 mmol, 73% yield). 1H NMR (500 MHz, CDCl3) δ 4.13-4.03 (m, 2H), 2.37-2.20 (m, 1H), 2.20-2.12 (m, 1H), 2.11-1.96 (m, 1H), 1.94-1.70 (m, 4H), 1.35-1.14 (m, 4H), 0.89-0.79 (m, 9H), 0.05-−0.11 (m, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08551984B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-09d7558bbcad488f8404b748a15b9211
출처 메모uspto-grants-2013_10