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Dimethylformamide → HCID 23035470, 화합물

HRID 1710086
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반응식

HRID 1710086 반응식
S(Cl)([Cl:3])=O.[N:5]1([CH2:11][C:12]2[CH:13]=[C:14]([CH:21]=[CH:22][CH:23]=2)[O:15][CH2:16][CH2:17][C:18](O)=[O:19])[CH2:10][CH2:9][CH2:8][CH2:7][CH2:6]1.CN(C)C=O>ClCCl>[ClH:3].[N:5]1([CH2:11][C:12]2[CH:13]=[C:14]([CH:21]=[CH:22][CH:23]=2)[O:15][CH2:16][CH2:17][C:18]([Cl:3])=[O:19])[CH2:10][CH2:9][CH2:8][CH2:7][CH2:6]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 24386Thionyl ChlorideHCID 154971Propanoic acid, 3-(3-(1-piperidinylmethyl)phenoxy)-

생성물 1

HCID 23035470HCID 23035470, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Thionyl chloride (23.8 g) was added slowly to a cooled (0° C.) mixture of 3-[3-(piperidinomethyl)phenoxy]propionic acid and dimethylformamide (0.5 ml) in dichloromethane (100 ml). The resulting suspension was stirred at room temperature overnight, and solvent was removed under reduced pressure to give 3-[3-(piperidinomethyl)phenoxy]propionyl chloride hydrochloride (18.9 g) as an oil.

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후처리

  1. temperaturea cooled
  2. customsolvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-bcfa00329ee74a6a9dd421b43f5b8a4c
출처 데이터셋
uspto-grants-1990_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04952589

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