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Dimethyl Sulfate → 1-Methyl-7-benzoylindole

HRID 236367
ノート
印刷プレビュー

反応式

HRID 236367 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

HCID 201894801-Methyl-7-benzoylindole

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-1e8d03e4135044db954668e7970b98d1
出典データセット
uspto-grants-1987_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04644005

反応ノート

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