Acetonitrile → 2-Amino-1-(4-chlorophenyl)ethan-1-one hydrochloride

HRID 908093

반응식

HRID 908093 반응식
Br[CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([Cl:11])=[CH:7][CH:6]=1)=[O:4].C(#[N:14])C>>[ClH:11].[NH2:14][CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([Cl:11])=[CH:7][CH:6]=1)=[O:4]

참가 물질

3

반응 조건

온도
105 °C

실험 절차

A mixture of 2-bromo-1-(4-chlorophenyl)ethanone (1.0 eq.) and NaN(CHO)2 (1.1 eq.) in acetonitrile (1.5 mL per mmol) was heated to reflux for 4 h at 105° C. ext. temperature. The formed sodium bromide was removed by filtration and the filtrate concentrated in vacuo. The residue was dissolved in ethanol (2.5 mL per mmol) and conc. aq. hydrochloric acid (0.9 mL per mmol) added at ambient temperature. After stirring for 72 h at room temperature the solids were filtered off and washed with ethanol (1×0.5 mL per mmol). Drying of the solids afforded 2-amino-1-(4-chlorophenyl)ethanone hydrochloride in ca. 50% yield that was used in the next step without purification.

후처리

  1. temperaturewas heated
  2. customThe formed sodium bromide was removed by filtration
  3. concentrationthe filtrate concentrated in vacuo
  4. dissolutionThe residue was dissolved in ethanol (2.5 mL per mmol)
  5. additionconc. aq. hydrochloric acid (0.9 mL per mmol) added at ambient temperature
  6. filtrationwere filtered off
  7. washwashed with ethanol (1×0.5 mL per mmol)
  8. customDrying of the solids

출처 및 근거

ORD 기록
ord-964b167cc6c84c37b09f3b27399e11ba
출처 데이터셋
uspto-grants-2011_09
특허 번호
US08017555B2

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