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Hydrochloric Acid → 7-hydroxy-2-phenyl-1H-benzoimidazole-4-carboxylic acid

HRID 349469
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반응식

HRID 349469 반응식
C[O:2][C:3]([C:5]1[C:13]2[N:12]=[C:11]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[NH:10][C:9]=2[C:8]([O:20]C)=[CH:7][CH:6]=1)=[O:4].[Cl-].[Al+3].[Cl-].[Cl-].Cl>C1(C)C=CC=CC=1>[OH:20][C:8]1[C:9]2[NH:10][C:11]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)=[N:12][C:13]=2[C:5]([C:3]([OH:4])=[O:2])=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 6451240Aluminum(III) ChlorideHCID 22663468Methyl 7-Methoxy-2-phenyl-1H-benzo[d]imidazole-4-carboxylate

생성물 1

HCID 583814087-hydroxy-2-phenyl-1H-benzoimidazole-4-carboxylic acid수율 86.4%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

7-methoxy-2-phenyl-1H-benzoimidazole-4-carboxylic acid methyl ester (4.5 g, 15.94 mmol) obtained in step 3 was dissolved in 100 ml of toluene, aluminum chloride (9.56 g, 71.73 mmol) was added thereto and refluxed for 8 hours. The resulting solution was cooled to room temperature, the reaction was stopped by adding 3 N HCl thereto and stirred for 30 min. The precipitate formed was filtered, washed with benzene and dried to obtain the title compound (3.5 g, 13.77 mmol) in a yield of 86%.

후처리

  1. temperaturerefluxed for 8 hours
  2. customThe precipitate formed
  3. filtrationwas filtered
  4. washwashed with benzene
  5. customdried

출처 및 근거

ORD 기록
ord-eabafe62ed674ac9afaa87a270ce7a78
출처 데이터셋
uspto-grants-2007_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07179832B2

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