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Thionyl Chloride → 1-Benzyl-2-chloromethyl-4,5-dimethylimidazole hydrochloride

HRID 65043
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인쇄 미리보기

반응식

HRID 65043 반응식
[CH2:1]([N:8]1[C:12]([CH3:13])=[C:11]([CH3:14])[N:10]=[C:9]1[CH2:15]O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.S(Cl)([Cl:19])=O>ClCCl>[ClH:19].[CH2:1]([N:8]1[C:12]([CH3:13])=[C:11]([CH3:14])[N:10]=[C:9]1[CH2:15][Cl:19])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 202350581-Benzyl-4,5-dimethyl-2-hydroxymethylimidazole

생성물 1

HCID 202350701-Benzyl-2-chloromethyl-4,5-dimethylimidazole hydrochloride

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

A suspension of 15 g (69 mmol) of 1-benzyl-4,5-dimethyl-2-hydroxymethylimidazole in 50 ml of dichloromethane was added portionwise over a period of 30 minutes to a stirred solution of 25 ml of thionyl chloride in 25 ml of dichloromethane. The solution obtained was boiled under reflux for 1.5 hours and then left to stand at room temperature overnight. Evaporation of the solution gave 23.5 g of crude 1-benzyl-2-chloromethyl-4,5-dimethylimidazole hydrochloride in the form of an oil which was used in the next step without further purification.

후처리

  1. customThe solution obtained
  2. temperatureunder reflux for 1.5 hours
  3. waitleft
  4. customEvaporation of the solution

출처 및 근거

ORD 기록
ord-3f551307f9ae4dd6afb0266168cd2c7e
출처 데이터셋
uspto-grants-1986_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04612324

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