Oxalyl chloride → Benzyl 4-(chlorocarbonyl)piperidine-1-carboxylate

HRID 79730

반응식

HRID 79730 반응식
[CH2:1]([O:8][C:9]([N:11]1[CH2:16][CH2:15][CH:14]([C:17]([OH:19])=O)[CH2:13][CH2:12]1)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(Cl)(=O)C([Cl:23])=O>ClCCl>[CH2:1]([O:8][C:9]([N:11]1[CH2:16][CH2:15][CH:14]([C:17]([Cl:23])=[O:19])[CH2:13][CH2:12]1)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

참가 물질

4

반응물 2

HCID 65578Oxalyl chlorideHCID 7364891-Carbobenzoxy-4-piperidinecarboxylic Acid

생성물 1

HCID 2776270Benzyl 4-(chlorocarbonyl)piperidine-1-carboxylate수율 101.8%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Piperidine-1,4-dicarboxylic acid monobenzyl ester (40.2 g, 0.15 mol) in dichloromethane (300 mL) was treated with oxalyl chloride (100 g, 0.79 mol). The reaction mixture was stirred at ambient temperature for 4 hours and the mixture was concentrated to afford crude 4-chlorocarbonyl-piperidine-1-carboxylic acid benzyl ester (43 g), which was used without further purification.

후처리

  1. concentrationthe mixture was concentrated

출처 및 근거

ORD 기록
ord-e041540c78f04ed5ae40a2c74ef0a5c9
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08841278B2

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