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Water → 6-Benzoxazolol, 2-(trifluoromethyl)-

HRID 1271824
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HRID 1271824 반응식
O[C:2]1[CH:7]=[C:6]([OH:8])[CH:5]=[CH:4][C:3]=1[NH:9][C:10](=[O:15])[C:11]([F:14])([F:13])[F:12].C1(C)C=CC(S(O)(=O)=O)=CC=1.O>C1(C)C=CC=CC=1>[F:14][C:11]([F:12])([F:13])[C:10]1[O:15][C:2]2[CH:7]=[C:6]([OH:8])[CH:5]=[CH:4][C:3]=2[N:9]=1
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참가 물질

5

반응물 3

HCID 962WaterHCID 6101p-Toluenesulfonic acidHCID 18454996N-(2,4-dihydroxyphenyl)-2,2,2-trifluoro-acetamide

생성물 1

HCID 184549866-Benzoxazolol, 2-(trifluoromethyl)-수율 40.8%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A stirred solution of 0.8 gram (0.0036) of N-(2,4-dihydroxyphenyl)-2,2,2-trifluoroacetamide and a catalytic amount of p-toluenesulfonic acid in 50 mL of toluene was heated at reflux during an 18 hour period while the theoretical amount of water by-product was collected in a Dean-Stark trap. After this time the reaction mixture was concentrated under reduced pressure to a residue. The residue was purified with column chromatography on silica gel using methylene chloride as an eluant. The appropriate fractions were combined and concentrated under reduced pressure, yielding 0.3 gram of the subject compound. The NMR spectrum was consistent with the proposed structure.

후처리

  1. customwas collected in a Dean-Stark trap
  2. concentrationAfter this time the reaction mixture was concentrated under reduced pressure to a residue
  3. customThe residue was purified with column chromatography on silica gel
  4. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-e8b1e945ae2243caabc427497c88209b
출처 데이터셋
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07208450B2

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