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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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m-Chloroperbenzoic acid → HCID 85040066, 화합물

HRID 1635859
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HRID 1635859 반응식
ClC1C=C(C=CC=1)C(OO)=[O:6].[Cl:12][C:13]1[CH:22]=[C:21]([C:23]#[C:24][CH2:25][N:26]([CH3:28])[CH3:27])[CH:20]=[CH:19][C:14]=1[C:15]([O:17][CH3:18])=[O:16]>ClCCl>[Cl:12][C:13]1[CH:22]=[C:21]([C:23](=[O:6])[CH:24]=[CH:25][N:26]([CH3:28])[CH3:27])[CH:20]=[CH:19][C:14]=1[C:15]([O:17][CH3:18])=[O:16]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 70297m-Chloroperbenzoic acidHCID 539792842-Chloro-4-(3-dimethylaminopropyn-1-yl)-benzoic acid methyl ester

생성물 1

HCID 85040066HCID 85040066, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
-20 °C

실험 절차

Gradually, 3-chloroperoxybenzoic acid (10.76 g) was added to a solution of 2-chloro-4-(3-dimethylamino-propyn-1yl)-benzoic acid, methyl ester (15.07 g in dichloromethane (40 ml), at a rate to maintain the reaction temperature at −20° C. The mixture was stirred for 10-15 minutes. The resulting N-oxide was purified by chromatography on Activity Grade I basic alumina (215 g), eluting with 10% methanol/dichloromethane. The solvent was evaporated in vacuo between 12 to 18° C. The resulting residue was dissolved in methanol (100 ml) and heated at 60-65° C. with stirring for 18 hours. After removing the solvent in vacuo, and the product was purified by column chromatography on silica gel (190 g), eluting with 70% ethyl acetate/hexane. Trituration with diethyl ether containing some hexane afforded the title compound as a solid (5.68 g), m.p. 92-96° C.

후처리

  1. customThe resulting N-oxide was purified by chromatography on Activity Grade I basic alumina (215 g)
  2. washeluting with 10% methanol/dichloromethane
  3. customThe solvent was evaporated in vacuo between 12 to 18° C
  4. dissolutionThe resulting residue was dissolved in methanol (100 ml)
  5. temperatureheated at 60-65° C.
  6. stirringwith stirring for 18 hours
  7. customAfter removing the solvent in vacuo
  8. customthe product was purified by column chromatography on silica gel (190 g)
  9. washeluting with 70% ethyl acetate/hexane

출처 및 근거

ORD 기록
ord-7b562549922444498e09ca1cfeba8d2d
출처 데이터셋
uspto-grants-2003_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06511974B1

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