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Dimethyl Sulfate → 1-Methyl-7-benzoylindole

HRID 236367
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HRID 236367 반응식
[C:1]([C:9]1[CH:10]=[CH:11][CH:12]=[C:13]2[C:17]=1[NH:16][CH:15]=[CH:14]2)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.S(OC)(O[CH3:22])(=O)=O.[OH-].[K+]>CC(C)=O>[CH3:22][N:16]1[C:17]2[C:13](=[CH:12][CH:11]=[CH:10][C:9]=2[C:1](=[O:8])[C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[CH:14]=[CH:15]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6497Dimethyl SulfateHCID 14797Potassium HydroxideHCID 10878711(1H-Indol-7-yl)(phenyl)methanone

생성물 1

HCID 201894801-Methyl-7-benzoylindole

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

A mixture of 8.57 g. (38.8 mmoles) of 7-benzoylindole, 5.38 g. (42.7 mmoles) of dimethyl sulfate and 5.12 g. of 85% potassium hydroxide in 40 ml. of acetone was heated to reflux for 75 minutes. The mixture was poured into 500 ml. of water and extracted with methylene chloride. The organic phase was separated, dried and concentrated. The residue was chromatographed on silica gel using methylene chloride-hexane as the eluant. The fractions containing the product were combined and concentrated to dryness, 6.5 g.

후처리

  1. additionA mixture of 8.57 g
  2. temperatureto reflux for 75 minutes
  3. additionThe mixture was poured into 500 ml
  4. extractionof water and extracted with methylene chloride
  5. customThe organic phase was separated
  6. customdried
  7. concentrationconcentrated
  8. customThe residue was chromatographed on silica gel
  9. additionThe fractions containing the product
  10. concentrationconcentrated to dryness, 6.5 g

출처 및 근거

ORD 기록
ord-1e8d03e4135044db954668e7970b98d1
출처 데이터셋
uspto-grants-1987_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04644005

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