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Butyric Acid → 4-Methyl-2-propyl-1H-benzimidazole

HRID 1636388
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HRID 1636388 반응식
[NH2:1][C:2]1[C:7]([NH2:8])=[CH:6][CH:5]=[CH:4][C:3]=1[CH3:9].[C:10](O)(=O)[CH2:11][CH2:12][CH3:13].[H-].[Na+].C(=O)([O-])[O-].[Na+].[Na+].C(=O)=O>O>[CH3:9][C:3]1[C:2]2[N:1]=[C:10]([CH2:11][CH2:12][CH3:13])[NH:8][C:7]=2[CH:6]=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 264Butyric AcidHCID 280Carbon DioxideHCID 10340Sodium CarbonateHCID 175932,3-DiaminotolueneHCID 24758Sodium hydride

생성물 1

HCID 219956454-Methyl-2-propyl-1H-benzimidazole

시약·촉매·용매 1

HCID 962
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
Water
용매

실험 절차

5.00 g (41 mmol) of 2,3-diamino-toluene and 3.7 ml (41 mmol) of butyric acid are stirred in 41 ml of polyphosphoric acid at 120° C. for 3 hours, and the mixture is poured into 410 ml of water and brought to pH=9 with solid sodium hydride. Thereafter, sodium carbonate is added until the evolution of carbon dioxide has ended, the mixture is extracted five times with 100 ml of ethyl acetate each time, the combined organic phases are dried with anhydrous sodium sulphate and the solution is evaportated - finally under a high vacuum; crude weight: 5.89 g.

후처리

  1. extractionthe mixture is extracted five times with 100 ml of ethyl acetate each time
  2. dry with materialthe combined organic phases are dried with anhydrous sodium sulphate

출처 및 근거

ORD 기록
ord-3c53f231a0d44376b1292d682755468c
출처 데이터셋
uspto-grants-2000_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06034115

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