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Ethanol → HCID 7035705, 화합물

HRID 1656326
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HRID 1656326 반응식
[CH2:1](O)[CH3:2].S(=O)(=O)(O)O.[C:9]([NH:17][C@H:18]([C:22]([OH:24])=[O:23])[CH:19]([CH3:21])[CH3:20])(=[O:16])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>>[C:9]([NH:17][C@H:18]([C:22]([O:24][CH2:1][CH3:2])=[O:23])[CH:19]([CH3:21])[CH3:20])(=[O:16])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 702EthanolHCID 1118Sulfuric AcidHCID 730290(2S)-3-methyl-2-(phenylformamido)butanoic acid

생성물 1

HCID 7035705HCID 7035705, 화합물수율 71%

실험 절차

Dissolve in 100 ml of ethanol 0.045 mol (10 g) of N-benzoylvaline obtained in the preceding Step, add 5 ml of concentrated sulphuric acid, then heat at reflux for 24 hours. Evaporate to dryness, take up in ether, wash with water then with a 10% potassium bicarbonate solution, dry, filter and evaporate to dryness. Ethyl N-benzoylvalinate is obtained.

후처리

  1. customobtained in the preceding Step
  2. temperatureheat
  3. temperatureat reflux for 24 hours
  4. customEvaporate to dryness
  5. washwash with water
  6. dry with materialwith a 10% potassium bicarbonate solution, dry
  7. filtrationfilter
  8. customevaporate to dryness

출처 및 근거

ORD 기록
ord-f32974852f14475aa494efe18e9dd3d6
출처 데이터셋
uspto-grants-1993_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05254548

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