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HCID 20073070, 화합물 → HCID 21429279, 화합물

HRID 437605
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HRID 437605 반응식
[CH:1]1([C:4]([C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([C:19]([F:22])([F:21])[F:20])[CH:14]=2)([OH:12])[CH2:5][CH2:6][N:7](C)[C:8](=O)C)[CH2:3][CH2:2]1.CC(C)([O-])C.[K+]>CS(C)=O>[CH:1]1([C:4]([C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([C:19]([F:20])([F:21])[F:22])[CH:14]=2)([OH:12])[CH2:5][CH2:6][NH:7][CH3:8])[CH2:2][CH2:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

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HCID 20073070HCID 20073070, 화합물HCID 23665647Potassium tert-butoxide

생성물 1

HCID 21429279HCID 21429279, 화합물

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

A mixture of 5 g. (0.016 mole) of 1-cyclopropyl-3-(N-methylacetamido)-1-(3-trifluoromethylphenyl)-1-propanol, 2.9 g. (0.024 mole) of potassium tertiary butoxide and 25 ml. of dimethyl sulfoxide was warmed on a steam bath for 45 minutes. The mixture was cooled, poured into ice water and extracted with benzene. The benzene extract was dried over magnesium sulfate and concentrated to an oil which was distilled at 108° C./0.15 mm. The yield was 2.6 g. (59%).

후처리

  1. additionA mixture of 5 g
  2. temperatureThe mixture was cooled
  3. extractionextracted with benzene
  4. extractionThe benzene extract
  5. dry with materialwas dried over magnesium sulfate
  6. concentrationconcentrated to an oil which
  7. distillationwas distilled at 108° C./0.15 mm

출처 및 근거

ORD 기록
ord-72b555bd542145f8ab0c436f32bf0c5a
출처 데이터셋
uspto-grants-1977_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04031245

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