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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

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl AlcoholHCID 244—
반응물Sodium IodideHCID 5238—
반응물3-Chloro-2,2-dimethylpropanoyl chlorideHCID 61345—
반응물DiisopropylethylamineHCID 81531—
반응물Tert-butyl (piperidin-4-ylmethyl)carbamateHCID 723429—
반응물Benzyl 3-chloropivalateHCID 54294282—
용매DimethylformamideHCID 6228—
생성물tert-Butyl [{1-(2-benzyloxycarbonyl-2-methylpropyl)piperidin-4-yl}methyl]carbamateHCID 866021211.3%

반응 조건

온도120 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737163B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-51017605c27a4df0905c4c42548db89d
출처 메모uspto-grants-2010_06