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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1-Bromo-3-chloropropane → 1-(3-Chloropropyl)indolin-2-one

HRID 1751037
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반응식

HRID 1751037 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][C:2]1=[O:10].Br[CH2:12][CH2:13][CH2:14][Cl:15].C(=O)([O-])[O-].[K+].[K+]>C(#N)C>[Cl:15][CH2:14][CH2:13][CH2:12][N:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][C:2]1=[O:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 80061-Bromo-3-chloropropaneHCID 11430Potassium CarbonateHCID 321710Oxindole

생성물 1

HCID 180699061-(3-Chloropropyl)indolin-2-one

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

Oxindole (2.00 g, 0.0150 mol), 1-bromo-3-chloropropane (2.97 mL, 0.03 mol), and potassium carbonate (4.15 g, 0.03 mol) in acetonitrile (40 mL) were heated at reflux for 20 hours. The mixture was evaporated, diluted with ethyl acetate, washed with 2M aqueous hydrochloric acid and brine, dried (MgSO4), and evaporated. The residue was purified by Biotage flash column chromatography (30% ethyl acetate/hexanes) to give product as an oil which solidified on standing (1.57 g, 50%); MS for C11H12ClNO m/z 210 (M+H)+.

후처리

  1. temperatureat reflux for 20 hours
  2. customThe mixture was evaporated
  3. additiondiluted with ethyl acetate
  4. washwashed with 2M aqueous hydrochloric acid and brine
  5. dry with materialdried (MgSO4)
  6. customevaporated
  7. customThe residue was purified by Biotage flash column chromatography (30% ethyl acetate/hexanes)
  8. customto give product as an oil which

출처 및 근거

ORD 기록
ord-6b3a8dd9ca414553ad553e3ccb4c6562
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09156840B2

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