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Sulfuryl chloride → HCID 19992468、化合物

HRID 345504
ノート
印刷プレビュー

反応式

HRID 345504 の反応式
[CH3:1][O:2][C:3](=[O:15])[CH2:4][CH2:5][C:6](=[O:14])[C:7]1[CH:12]=[CH:11][C:10]([Cl:13])=[CH:9][CH:8]=1.S(Cl)([Cl:19])(=O)=O>ClCCl>[Cl:19][CH:5]([C:6](=[O:14])[C:7]1[CH:8]=[CH:9][C:10]([Cl:13])=[CH:11][CH:12]=1)[CH2:4][C:3]([O:2][CH3:1])=[O:15]
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 24648Sulfuryl chlorideHCID 230774Methyl 4-(4-chlorophenyl)-4-oxobutanoate

生成物 1

HCID 19992468HCID 19992468、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

A solution of 179 g (0.79 mole) of methyl-3-(4-chlorobenzoyl)propionate in 175 mL of dichloromethane was cooled to 0° and treated dropwise with 69.8 mL (117.3 g; 0.86 mole, d=1.68) of sulfuryl chloride. After the addition was complete, the cold bath was removed, and the reaction mixture was allowed to warm to room temperature while stirring overnight. The mixture was treated with 100 mL of water and basified cautiously with 50% sodium hydroxide. The layers were separated, the dichloromethane layer dried over magnesium sulfate and evaporated under reduced pressure (245.3 g). The residue was purified by vacuum distillation (135° C./0.3 mm) to obtain three fractions for a total of 198.6 g (96%).

後処理

  1. additionAfter the addition
  2. customthe cold bath was removed
  3. additionThe mixture was treated with 100 mL of water and basified cautiously with 50% sodium hydroxide
  4. customThe layers were separated
  5. dry with materialthe dichloromethane layer dried over magnesium sulfate
  6. customevaporated under reduced pressure (245.3 g)
  7. distillationThe residue was purified by vacuum distillation (135° C./0.3 mm)
  8. customto obtain three fractions for a total of 198.6 g (96%)

出典と根拠

ORDレコード
ord-0a9e9c142d6b4389bc168c3d76ca0624
出典データセット
uspto-grants-1991_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05057534

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート