참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Ethyl formate | HCID 8025 | — |
| 반응물 | Tert-butyl 1-oxo-8-azaspiro(4.5)decane-8-carboxylate | HCID 10848487 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | tert-Butyl 2-(hydroxymethyl)-1-oxo-8-azaspiro[4.5]decane-8-carboxylate | HCID 21983946 | 51.4% |
반응 단계
tert-Butyl 1-oxo-8-azaspiro[4.5]decane-8-carboxylate from Procedure 1, Step G (0.526 g, 2.08 mmol) was dried by evaporating with toluene (10 mL) three times in vacuo, dissolved in methyl-tert-butyl ether (5 mL), and cooled to −78° C. To this solution was added ethyl formate (0.336 mL, 4.15 mmol) and then potassium t-butoxide (0.466 g, 4.16 mmol). After 2 days, the reaction mixture was diluted with diethyl ether, poured into 2N HCl, and extracted three times with diethyl ether. The organic layers were combined, washed with brine, dried over sodium sulfate, filtered, and concentrated to afford 0.575 g. The residue was purified by flash chromatography eluting with 45% ethyl acetate/hexanes to give the title compound (0.303 g). MS/EI (acetonitrile/water): m/z 304 (M+1+Na) retention time=2.9 min.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07091211B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-01aabc2e796f428ba758c5068521a6d6 |
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| 출처 메모 | uspto-grants-2006_08 |
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