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Trifluoroacetic acid → (S)-2-amino-N,N-dimethyl-3-phenylpropanamide

HRID 1879465
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반응식

HRID 1879465 반응식
C(OC(=O)[NH:7][C@H:8]([C:16](=[O:20])[N:17]([CH3:19])[CH3:18])[CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)(C)(C)C.FC(F)(F)C(O)=O>C(Cl)Cl>[NH2:7][C@@H:8]([CH2:9][C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1)[C:16]([N:17]([CH3:19])[CH3:18])=[O:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 14541824tert-Butyl (S)-(1-(dimethylamino)-1-oxo-3-phenylpropan-2-yl)carbamate

생성물 1

HCID 11008771(S)-2-amino-N,N-dimethyl-3-phenylpropanamide수율 76%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

((S)-1-Dimethylcarbamoyl-2-phenyl-ethyl)-carbamic acid tert-butyl ester (2.0 g, 6.85 mmol) was dissolved in methylene chloride (20 mL) at 0° C. Trifluoroacetic acid (20 mL) was added. The mixture was stirred for 2 h and evaporated. The residue was dissolved in methylene chloride and very carefully basified using saturated aqueous sodium bicarbonate. The organic layer was separated and the aqueous layer was extracted using methylene chloride. The combined organic extracts were washed with water and brine, and then dried over sodium sulfate to give (S)-2-amino-N,N-dimethyl-3-phenyl-propionamide (1.0 g, 76%) as yellow oil.

후처리

  1. customevaporated
  2. dissolutionThe residue was dissolved in methylene chloride
  3. customThe organic layer was separated
  4. extractionthe aqueous layer was extracted
  5. washThe combined organic extracts were washed with water and brine
  6. dry with materialdried over sodium sulfate

출처 및 근거

ORD 기록
ord-358dc480b1dc4c308e745e2478c890fb
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08314250B2

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