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Chloroacetamide → N~2~-(Diphenylmethyl)glycinamide

HRID 1197887
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HRID 1197887 반응식
[C:1]1([CH:7]([NH2:14])[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl[CH2:16][C:17]([NH2:19])=[O:18].C(=O)(O)[O-].[Na+]>C(O)C>[C:1]1([CH:7]([NH:14][CH2:16][C:17]([NH2:19])=[O:18])[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6580ChloroacetamideHCID 7036BenzhydrylamineHCID 516892Sodium Bicarbonate

생성물 1

HCID 319782N~2~-(Diphenylmethyl)glycinamide

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A reaction vessel was charged with 18.3 g (100 mmole) of diphenylmethylamine dissolved in 250 ml of ethanol. Then a mixture of 9.35 g (100 mmole) of chloroacetamide and 8.4 g (100 mmole) of sodium bicarbonate was added and the suspension was brought to reflux and held at reflux for 3 days. Solvent was evaporated under reduced pressure and the residue was dissolved in dichloromethane. The organic phase was washed with water, dried over potassium carbonate and solvent was evaporated. The resulting solid crystallized from a mixture of benzene and cyclohexane.

후처리

  1. additionwas added
  2. temperatureto reflux
  3. temperatureat reflux for 3 days
  4. customSolvent was evaporated under reduced pressure
  5. dissolutionthe residue was dissolved in dichloromethane
  6. washThe organic phase was washed with water
  7. dry with materialdried over potassium carbonate and solvent
  8. customwas evaporated
  9. customThe resulting solid crystallized from a mixture of benzene and cyclohexane

출처 및 근거

ORD 기록
ord-7fe1206630344099a7a079b2e5bad12a
출처 데이터셋
uspto-grants-1994_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05278191

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