Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16602생성일: 2026년 10월 26일
Benzyl Alcohol → tert-Butyl [{1-(2-benzyloxycarbonyl-2-methylpropyl)piperidin-4-yl}methyl]carbamate
https://huagongshe.com/reaction/16602
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzyl Alcohol | HCID 244 | — |
| 반응물 | Sodium Iodide | HCID 5238 | — |
| 반응물 | 3-Chloro-2,2-dimethylpropanoyl chloride | HCID 61345 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Tert-butyl (piperidin-4-ylmethyl)carbamate | HCID 723429 | — |
| 반응물 | Benzyl 3-chloropivalate | HCID 54294282 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | tert-Butyl [{1-(2-benzyloxycarbonyl-2-methylpropyl)piperidin-4-yl}methyl]carbamate | HCID 86602121 | 1.3% |
반응 단계
To a stirred solution of tert-butyl (piperidin-4-ylmethyl)carbamate (38.8 g, 181 mmol) in N,N-dimethylformamide (100 mL) was added benzyl 3-chloropivalate {14.2 g, 124 mmol, prepared from 3-chloropivaloyl chloride (25.6 g, 165 mmol) and benzyl alcohol (19.6 g, 181 mmol), ethyldiisopropylamine (64.0 g, 495 mmol) and sodium iodide (27.1 g, 181 mmol) at ambient temperature. The resulting mixture was stirred at 120° C. for 14 h. The volatile components were removed by evaporation and the resulting residue was chromatographed on a column of silica gel eluting with hexane/ethyl acetate (1:1) to give 640 mg (1%) of the title compound as a pale yellow oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07737163B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-51017605c27a4df0905c4c42548db89d |
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| 출처 메모 | uspto-grants-2010_06 |
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