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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → 2-Bromo-N-methyl-N-phenylacetamide

HRID 2192364
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HRID 2192364 반응식
[CH3:1][NH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.C(=O)([O-])[O-].[K+].[K+].[Br:15][CH2:16][C:17](Br)=[O:18].O>ClCCl>[Br:15][CH2:16][C:17]([N:2]([CH3:1])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1)=[O:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 7515N-MethylanilineHCID 11430Potassium CarbonateHCID 61147Bromoacetyl bromide

생성물 1

HCID 344952-Bromo-N-methyl-N-phenylacetamide

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a mixture of N-methyl aniline (5 mL) and potassium carbonate (9.6 g) in 100 mL dichloromethane was added bromoacetyl bromide (8.1 mL) (exotherm). The mixture was stirred for 4.5h then water was added. The phases were separated and the organic layer was concentrated. The crude product was purified by silica gel chromatography eluting with 0-100% EtOAc/cyclohexane. The relevant fractions were combined and evaporated and the residue was taken up in dichloromethane and washed with water. The organic layer was stirred with another portion of water for a few minutes and then the layers were separated. Evaporation of the organic layer gave the sub-titled compound (10.2 g) as a straw coloured solid.

후처리

  1. customThe phases were separated
  2. concentrationthe organic layer was concentrated
  3. customThe crude product was purified by silica gel chromatography
  4. washeluting with 0-100% EtOAc/cyclohexane
  5. customevaporated
  6. washwashed with water
  7. customthe layers were separated
  8. customEvaporation of the organic layer

출처 및 근거

ORD 기록
ord-5872088bc0a441e9ad9dacb7f454debf
출처 데이터셋
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08329729B2

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