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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl 2-oxo-4-oxa-8-azaspiro[4.5]decane-8-carboxylate | HCID 10082452 | — |
| 반응물 | HCID 178419644 | HCID 178419644 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Ethyl 3-hydroxy-3-(2-phenylethynyl)-1-oxa-8-azaspiro[4.5]decane-8-carboxylate | HCID 57493817 | 87.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08580962B2 |
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| 출처 데이터셋 | uspto-grants-2013_11 |
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| ORD ID | ord-6ac54eb5fe97458d915fec7bffe53092 |
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| 출처 메모 | uspto-grants-2013_11 |
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