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2-Butylbenzofuran → 2-n-Butyl-3-(3'-methyl-4'-methoxybenzoyl)benzofuran

HRID 1283637
ノート
印刷プレビュー

反応式

HRID 1283637 の反応式
[CH3:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[O:11][CH3:12])[C:5](Cl)=[O:6].[CH2:13]([C:17]1[O:18][C:19]2[CH:25]=[CH:24][CH:23]=[CH:22][C:20]=2[CH:21]=1)[CH2:14][CH2:15][CH3:16]>C(=S)=S>[CH2:13]([C:17]1[O:18][C:19]2[CH:25]=[CH:24][CH:23]=[CH:22][C:20]=2[C:21]=1[C:5](=[O:6])[C:4]1[CH:8]=[CH:9][C:10]([O:11][CH3:12])=[C:2]([CH3:1])[CH:3]=1)[CH2:14][CH2:15][CH3:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 779512-ButylbenzofuranHCID 210929304-Methoxy-3-methylbenzoyl chloride

生成物 1

HCID 215186372-n-Butyl-3-(3'-methyl-4'-methoxybenzoyl)benzofuran

試薬・触媒・溶媒 1

HCID 6348Carbon Disulfide溶媒

実験手順

To a cooled, stirred solution of 10.8 g. (0.058 mol.) of 3-methyl-4-methoxybenzoic acid chloride and 9.4 g. (0.054 mol.) of 2-n-butylbenzofuran in 40 ml. of carbon disulfide was added dropwise over a 20 minute interval 28.2 g. (0.108 mol.) of stannic chloride. After addition, the reaction mixture was warmed to ambient temperature and stirred for two hours. The mixture was then poured onto 100 ml. of ice-water and stirred for one hour. The solvent was removed, the product extracted into chloroform and the extracts were washed with water, dried (Na2SO4) and concentrated in vacuo to give 2-n-butyl-3-(3'-methyl-4'-methoxybenzoyl)benzofuran.

後処理

  1. additionAfter addition
  2. stirringstirred for two hours
  3. additionThe mixture was then poured onto 100 ml
  4. customThe solvent was removed
  5. extractionthe product extracted into chloroform
  6. washthe extracts were washed with water
  7. dry with materialdried (Na2SO4)
  8. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-01bb8d5f5e7d4279bbda5d1748e0f8d5
出典データセット
uspto-grants-1976_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03975537

反応ノート

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