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Water → phenyl N-(4-benzoylphenyl)carbamate

HRID 480046
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HRID 480046 반응식
[NH2:1][C:2]1[CH:15]=[CH:14][C:5]([C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[O:7])=[CH:4][CH:3]=1.[C:16](Cl)(=[O:24])[O:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1.O>N1C=CC=CC=1>[C:6]([C:5]1[CH:4]=[CH:3][C:2]([NH:1][C:16](=[O:24])[O:17][C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)=[CH:15][CH:14]=1)(=[O:7])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 143464-AminobenzophenoneHCID 15891Phenyl chloroformate

생성물 1

HCID 15548170phenyl N-(4-benzoylphenyl)carbamate수율 110.8%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

To 4-aminobenzophenone (1.97 g) dissolved in pyridine (50 mL), phenyl chlorocarbonate (1.38 g) was added at 0° C. and the mixture was stirred at room temperature for 1 hour. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was dried over anhydrous Na2SO4 and evaporated. The residue was purified by column chromatography on silica gel (hexane/ethyl acetate=4/1 to 1/2) to give the subject compound (3.1 g).

후처리

  1. extractionextracted with ethyl acetate
  2. dry with materialThe organic layer was dried over anhydrous Na2SO4
  3. customevaporated
  4. customThe residue was purified by column chromatography on silica gel (hexane/ethyl acetate=4/1 to 1/2)

출처 및 근거

ORD 기록
ord-34151b7df0284bec9390963ddd138333
출처 데이터셋
uspto-grants-2003_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06649624B2

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