Toluene → 0-cyclopropylmethyl N-phenylacetyl-(2,6-dichlorophenyl)-acetamidoxime

HRID 2212058노트

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HRID 2212058 반응식
C1(C[C:5]2([Cl:17])[CH:10]=[CH:9][CH:8]=[C:7]([Cl:11])[CH:6]2[CH2:12][C:13](=[N:15][OH:16])[NH2:14])CC1.[C:18]1([CH2:24][C:25](Cl)=[O:26])[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1.C(=O)([O-])O.[Na+].[C:33]1([CH3:39])[CH:38]=[CH:37]C=CC=1>>[CH:38]1([CH2:37][C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][C:18]=2[CH2:24][C:25]([NH:14][C:13](=[N:15][OH:16])[CH2:12][C:6]2[C:7]([Cl:11])=[CH:8][CH:9]=[CH:10][C:5]=2[Cl:17])=[O:26])[CH2:33][CH2:39]1

참가 물질

5

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온도
100 °C

실험 절차

5.0 g (18 mmol) of 0-cyclopropylmethyl (2,6-dichlorophenyl)acetamidoxime in 40 ml of toluene were heated to 85° C and admixed with 3.9 g (25 mmol) of phenylacetyl chloride. The mixture was heated at 100° C. for 5 h, cooled, poured into aqueous sodium hydrogen carbonate solution (pH 7) and extracted three times with toluene. The combined extracts were washed with water, dried over sodium sulfate and concentrated under reduced pressure. The crude product (5.6 g) was purified by silica gel chromatography using cyclohexane/ethyl acetate. M.p. 134–135° C.

후처리

  1. temperaturecooled
  2. extractionextracted three times with toluene
  3. washThe combined extracts were washed with water
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe crude product (5.6 g) was purified by silica gel chromatography

출처 및 근거

ORD 기록
ord-e65edce304774709b9289615e9c9e9ef
출처 데이터셋
uspto-grants-2006_09
특허 번호
US07101900B2

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