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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2040851생성일: 2026년 10월 27일

Ethyl 2-oxo-4-oxa-8-azaspiro[4.5]decane-8-carboxylate → Ethyl 3-hydroxy-3-(2-phenylethynyl)-1-oxa-8-azaspiro[4.5]decane-8-carboxylate

https://huagongshe.com/reaction/2040851

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl 2-oxo-4-oxa-8-azaspiro[4.5]decane-8-carboxylateHCID 10082452—
반응물HCID 178419644HCID 178419644—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 3-hydroxy-3-(2-phenylethynyl)-1-oxa-8-azaspiro[4.5]decane-8-carboxylateHCID 5749381787.2%

반응 단계

To a solution of ethyl 2-oxo-4-oxa-8-azaspiro[4.5]decane-8-carboxylate (Edwin S. C. Wu, Ronald C. Griffith, James T. Loch III, Alex Kover, Robert J. Murray, George B. Mullen, James C. Blosser, Anthony C. Machulskis, Sally A. McCreedy, J. Med. Chem., 1995, 38 (9), pp 1558-1570, 82 mg, 0.362 mmol) in THF (4 mL) was added dropwise a 1M solution of phenylethynylmagnesium bromide in THF (0.724 mL, 0.724 mmol), stirring at r.t. under anhydrous nitrogen atmosphere. The reaction mixture was stirred at r.t. for 4 h, then at 60° C. for 6 h, then it was quenched with a saturated aqueous solution of ammonium chloride, extracted with EtOAc. The combined organic layers were washed with brine, dried over sodium sulphate and evaporated to dryness in vacuo. The crude was purified by automated flash chromatography (SP1®TM-Biotage; gradient Petroleum Ether-EtOAc from 75:25 to 4:6) affording the title product as yellow solid. Yield: 87.2%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08580962B2
출처 데이터셋uspto-grants-2013_11
ORD IDord-6ac54eb5fe97458d915fec7bffe53092
출처 메모uspto-grants-2013_11