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4-(1-Hydroxyethyl)-1-(dimethylethoxycarbonyl)imidazole → tert-butyl 4-acetyl-1H-imidazole-1-carboxylate

HRID 2213672
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인쇄 미리보기

반응식

HRID 2213672 반응식
[OH:1][CH:2]([C:4]1[N:5]=[CH:6][N:7]([C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH:8]=1)[CH3:3]>C(Cl)Cl.O=[Mn]=O>[C:2]([C:4]1[N:5]=[CH:6][N:7]([C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH:8]=1)(=[O:1])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 219577164-(1-Hydroxyethyl)-1-(dimethylethoxycarbonyl)imidazole

생성물 1

HCID 21957605tert-butyl 4-acetyl-1H-imidazole-1-carboxylate수율 46.4%

시약·촉매·용매 2

HCID 14801Manganese dioxide촉매HCID 6344Dichloromethane용매

실험 절차

4-(1-Hydroxyethyl)-1-(dimethylethoxycarbonyl)imidazole (8.7 g, 41 mmol) was dissolved in methylene chloride (100 mL) and MnO2 (10.7 g, 123 mmol) was added. The resulting reaction mixture was stirred overnight at ambient temperature. The reaction mixture was filtered, concentrated, and purified with silica column chromatography to afford 4 g of 4-acetyl-1-(dimethylethoxycarbonyl)imidazole and unreacted starting material.

후처리

  1. customThe resulting reaction mixture
  2. filtrationThe reaction mixture was filtered
  3. concentrationconcentrated
  4. custompurified with silica column chromatography

출처 및 근거

ORD 기록
ord-fee662d6d17347dd8b9e68680efda31c
출처 데이터셋
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07105563B2

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