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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

반응식

참여 물질

역할이름HCID투입량
반응물2-Bromo-1,2-diphenylethan-1-oneHCID 102630—
반응물SodiumHCID 5360545—
반응물1-(3-Benzyloxybenzoyl)-2-piperidinecarboxylic acidHCID 18367416—
촉매Sulfuric AcidHCID 1118—
용매EthanolHCID 702—
생성물2-Oxo-1,2-diphenylethyl 1-(3-benzyloxybenzoyl)-2-piperidinecarboxylateHCID 5424785628.4%

반응 조건

온도70 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06300344B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-969536c747cd4b3a94fb701bec284060
출처 메모uspto-grants-2001_10