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Bromoacetic Acid → HCID 66747421, 화합물

HRID 1019985
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반응식

HRID 1019985 반응식
Br[CH2:2][C:3]([OH:5])=[O:4].[CH3:6][O:7][C:8]1[C:9]([N+:17]([O-:19])=[O:18])=[C:10]([NH2:16])[CH:11]=[CH:12][C:13]=1[O:14][CH3:15]>>[CH3:6][O:7][C:8]1[C:9]([N+:17]([O-:19])=[O:18])=[C:10]([NH:16][CH2:2][C:3]([OH:5])=[O:4])[CH:11]=[CH:12][C:13]=1[O:14][CH3:15]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 6227Bromoacetic AcidHCID 10584093HCID 10584093, 화합물

생성물 1

HCID 66747421HCID 66747421, 화합물수율 68%

반응 조건

온도
58 °C

실험 절차

Bromoacetic acid (0.876 g, 6.31 mmol, 0.5 eq) is added portionwise to 3,4-dimethoxy-2-nitro-phenylamine (2.5 g, 12.61 mmol, 1.0 eq) and the mixture is stirred at 58° C. for 16 hours. The reaction is then quenched by 25% ammonia in water and diluted with water. The solid is filtered off and washed with 10% ammonia in water. The combined solutions are acidified by concentrated hydrochloric acid and the resulting precipitate is collected by filtration, washed with water and dried under vacuum to afford (3,4-dimethoxy-2-nitro-phenylamino)-acetic acid as a red solid (1.1 g, 34% yield).

후처리

  1. custom
The reaction is then quenched by 25% ammonia in water
  • additiondiluted with water
  • filtrationThe solid is filtered off
  • washwashed with 10% ammonia in water
  • filtrationthe resulting precipitate is collected by filtration
  • washwashed with water
  • customdried under vacuum
  • 출처 및 근거

    ORD 기록
    ord-23e169605e834739972f56fd7c3b89aa
    출처 데이터셋
    uspto-grants-2014_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08716280B2

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