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Hydrochloric Acid → 3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzoic acid

HRID 71138
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HRID 71138 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:10]=[CH:11][C:12]=1[N:13]1[CH:17]=[C:16]([CH3:18])[N:15]=[CH:14]1)[C:6]([O:8]C)=[O:7].Cl.O>[OH-].[Na+].CO>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:10]=[CH:11][C:12]=1[N:13]1[CH:17]=[C:16]([CH3:18])[N:15]=[CH:14]1)[C:6]([OH:8])=[O:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 962WaterHCID 27282443Methyl 3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzoate

생성물 1

HCID 579317633-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzoic acid수율 53.5%

시약·촉매·용매 2

HCID 887Methanol용매HCID 14798Sodium Hydroxide
용매

실험 절차

A mixture of methyl 3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzoate (16.0 g) in 2N aqueous sodium hydroxide solution (65 mL) and methanol (100 mL) was stirred at room temperature for 1 hr, and the mixture was acidified with 6N hydrochloric acid (pH=3-4). Water was added to the reaction mixture, and the precipitate was collected by filtration. The solid was washed with ethyl acetate and water to give the title compound (8.07 g). To the filtrate was added saturated brine, and the mixture was extracted with ethyl acetate/2-propanol. The organic layers were combined, washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was washed with ethyl acetate to give the title compound (4.10 g).

후처리

  1. filtrationthe precipitate was collected by filtration
  2. washThe solid was washed with ethyl acetate and water

출처 및 근거

ORD 기록
ord-4e4af118e7b543ea9d0037ac2595de57
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08822699B2

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