Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 380128생성일: 2026년 10월 25일
2-Bromo-1,2-diphenylethan-1-one → 2-Oxo-1,2-diphenylethyl 1-(3-benzyloxybenzoyl)-2-piperidinecarboxylate
https://huagongshe.com/reaction/380128
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Bromo-1,2-diphenylethan-1-one | HCID 102630 | — |
| 반응물 | Sodium | HCID 5360545 | — |
| 반응물 | 1-(3-Benzyloxybenzoyl)-2-piperidinecarboxylic acid | HCID 18367416 | — |
| 촉매 | Sulfuric Acid | HCID 1118 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 2-Oxo-1,2-diphenylethyl 1-(3-benzyloxybenzoyl)-2-piperidinecarboxylate | HCID 54247856 | 28.4% |
반응 단계
Sodium (54 mg) was dissolved in ethanol (8.0 ml), and then 1-(3-benzyloxybenzoyl)-2-piperidinecarboxylic acid (665 mg), conc. sulfuric acid (1 drop), and desyl bromide (539 mg) was successively dissolved thereto. The resulting mixture was stirred at 70° C. for 2 days, cooled to room temperature, and partitioned between ethyl acetate and 1N HCl. The organic layer was washed with 1N HCl, aqueous sodium bicarbonate, and brine, dried over MgSO4, and evaporated in vacuo. The residue was chromatographed over silica gel to afford 2-oxo-1,2-diphenylethyl 1-(3-benzyloxybenzoyl)-2-piperidinecarboxylate (297 mg) as a pale yellow oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06300344B1 |
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| 출처 데이터셋 | uspto-grants-2001_10 |
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| ORD ID | ord-969536c747cd4b3a94fb701bec284060 |
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| 출처 메모 | uspto-grants-2001_10 |
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