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Methane → 1-(4-Fluorophenyl)-1H-imidazole-4-carboxylic acid

HRID 447214
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HRID 447214 반응식
C([O:3][C:4]([C:6]1[N:7]=[CH:8][N:9]([C:11]2[CH:16]=[CH:15][C:14]([F:17])=[CH:13][CH:12]=2)[CH:10]=1)=[O:5])C.C>O1CCOCC1.[OH-].[Na+]>[F:17][C:14]1[CH:13]=[CH:12][C:11]([N:9]2[CH:10]=[C:6]([C:4]([OH:5])=[O:3])[N:7]=[CH:8]2)=[CH:16][CH:15]=1
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참가 물질

5

반응물 2

HCID 297MethaneHCID 17390092HCID 17390092, 화합물

생성물 1

HCID 173900481-(4-Fluorophenyl)-1H-imidazole-4-carboxylic acid

시약·촉매·용매 2

HCID 14798Sodium Hydroxide용매HCID 312751,4-Dioxane용매

실험 절차

Crude 1-(4-fluoro-phenyl)-1H-imidazole-4-carboxylic acid ethyl ester (175 mmol) was dissolved in 450 mL dioxane and 450 mL 2N sodium hydroxide solution. The reaction mixture was refluxed for 2 h. Charcoal (1 g, Norit SA II) was added and reflux was continued for another 20 min. The mixture was filtered hot and washed with 50 mL 2N sodium hydroxide solution. The filtrate was treated with 550 mL 2N HCl and stirred at room temperature overnight. The solid material was filtered off and dried at 50° C. and 15 mbar. The desired compound was obtained as an off-white solid (28 g, 78%), MS: m/e 205.1 (M−H).

후처리

  1. temperatureThe reaction mixture was refluxed for 2 h
  2. temperaturereflux
  3. filtrationThe mixture was filtered hot
  4. washwashed with 50 mL 2N sodium hydroxide solution
  5. additionThe filtrate was treated with 550 mL 2N HCl
  6. filtrationThe solid material was filtered off
  7. customdried at 50° C.

출처 및 근거

ORD 기록
ord-bd06e6e942904a0bafdcaa2420f5e1be
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08481548B2

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