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Acetic Anhydride → Ethyl 2',4'-difluoro-4-acetyloxy-5-iodo-[1,1']biphenyl-3-carboxylate

HRID 915617
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HRID 915617 반응식
[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[C:9]1[CH:19]=[C:13]([C:14]([O:16][CH2:17][CH3:18])=[O:15])[C:12]([OH:20])=[C:11]([I:21])[CH:10]=1.[C:22](OC(=O)C)(=[O:24])[CH3:23]>N1C=CC=CC=1>[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[C:9]1[CH:10]=[C:11]([I:21])[C:12]([O:20][C:22](=[O:24])[CH3:23])=[C:13]([C:14]([O:16][CH2:17][CH3:18])=[O:15])[CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 11407027Ethyl 5-(2,4-difluorophenyl)-3-iodo-salicylate

생성물 1

HCID 11442200Ethyl 2',4'-difluoro-4-acetyloxy-5-iodo-[1,1']biphenyl-3-carboxylate

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

A mixture of 500 mg (1.24 mmol) of ethyl 5-(2,4-difluorophenyl)-3-iodo-salicylate (Example 10) in 12 ml of pyridine and 3 ml of acetic anhydride was heated in a water bath for 20 min. The mixture was allowed to cool and poured over ice and the product was extracted with dichloromethane. After drying the organic phase and after evaporating the solvent at low pressure, the crude was recrystalized.

후처리

  1. temperaturewas heated in a water bath for 20 min
  2. temperatureto cool
  3. additionpoured over ice
  4. extractionthe product was extracted with dichloromethane
  5. customAfter drying the organic phase
  6. customafter evaporating the solvent at low pressure
  7. customthe crude was recrystalized

출처 및 근거

ORD 기록
ord-01e5f2b5d5f34d26ab670de74d1af477
출처 데이터셋
uspto-grants-2007_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07265245B2

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