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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Thionyl Chloride → 4-(chloromethyl)-1-ethyl-5-methyl-1H-imidazole hydrochloride

HRID 630122
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HRID 630122 반응식
[CH2:1]([N:3]1[C:7]([CH3:8])=[C:6]([CH2:9]O)[N:5]=[CH:4]1)[CH3:2].S(Cl)([Cl:13])=O>ClCCl>[ClH:13].[Cl:13][CH2:9][C:6]1[N:5]=[CH:4][N:3]([CH2:1][CH3:2])[C:7]=1[CH3:8]
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참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 54437975(1-ethyl-5-methyl-1H-imidazol-4-yl)methanol

생성물 1

HCID 668207564-(chloromethyl)-1-ethyl-5-methyl-1H-imidazole hydrochloride수율 96%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of (1-ethyl-5-methyl-1H-imidazol-4-yl)methanol (340 mg, 2.4 mmol) in anhydrous dichloromethane (20 mL) was added thionyl chloride (9004). The mixture was stirred at room temperature for 4 hours. Dichloromethane was evaporated, and the mixture was then co-evaporated with toluene (20 mL). The residue was dried in vacuo, affording 4-(chloromethyl)-1-ethyl-5-methyl-1H-imidazole hydrochloride (450 mg, 96% yield). The product was used without further purification.

후처리

  1. customDichloromethane was evaporated
  2. customThe residue was dried in vacuo

출처 및 근거

ORD 기록
ord-cc89ecf106494109b81b39669a90c7eb
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09315521B2

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