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Toluene → HCID 20535994、化合物

HRID 1075495
ノート
印刷プレビュー

反応式

HRID 1075495 の反応式
Cl[CH2:2][CH2:3][S:4]([C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([N+:13]([O-:15])=[O:14])[CH:8]=1)(=[O:6])=[O:5].C1(C)C=CC=CC=1.C(=O)([O-])[O-].[K+].[K+]>C(N(CC)CC)C.O>[N+:13]([C:9]1[CH:8]=[C:7]([S:4]([CH:3]=[CH2:2])(=[O:6])=[O:5])[CH:12]=[CH:11][CH:10]=1)([O-:15])=[O:14]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 1140TolueneHCID 11430Potassium CarbonateHCID 434616951-(beta-Chloroethylsulfonyl)-3-nitrobenzene

生成物 1

HCID 20535994HCID 20535994、化合物収率 94.3%

試薬・触媒・溶媒 2

HCID 8471Triethylamine触媒HCID 962Water溶媒

反応条件

温度
40 °C

実験手順

1-(β-chloroethylsulfonyl)-3-nitrobenzene (2.50 g, 10 mmol) was added to 20 g of toluene, to this solution were added 1.50 g of 49% aqueous potassium carbonate solution (potassium carbonate 5.3 mmol) and 50 mg (0.5 mmol) of triethylamine, and the mixture was stirred for 2 hours at 40° C. Then, 10 g of water was added and the mixture was separated to an organic phase and aqueous phase. This aqueous phase was extracted by chloroform, and the resulted organic phase was combined with the previous organic phase, dried over magnesium sulfate, the solvents were distilled off, to obtain 2.00 g (yield 94.3%) of (3-nitrophenyl)vinylsulfone.

後処理

  1. customthe mixture was separated to an organic phase and aqueous phase
  2. extractionThis aqueous phase was extracted by chloroform
  3. dry with materialdried over magnesium sulfate
  4. distillationthe solvents were distilled off

出典と根拠

ORDレコード
ord-3d29567437e34bdcbf7054ae5276ff58
出典データセット
uspto-grants-1999_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05902905

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート