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Bromine → (4-Bromo-2,3-dimethylphenyl)(methyl)sulfane

HRID 434229
ノート
印刷プレビュー

反応式

HRID 434229 の反応式
[CH3:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][C:3]=1[S:9][CH3:10].[Br:11]Br>C(O)(=O)C>[CH3:8][C:7]1[C:2]([CH3:1])=[C:3]([S:9][CH3:10])[CH:4]=[CH:5][C:6]=1[Br:11]
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 24408BromineHCID 214853032,3-Dimethylphenyl methyl sulfide

生成物 1

HCID 18757276(4-Bromo-2,3-dimethylphenyl)(methyl)sulfane

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒2 回

実験手順

510 g (3.33 mol) of 2,3-dimethylthioanisole are initially charged in 3 l of glacial acetic acid, and a solution of 592 g (7.4 mol) of bromine in 1 l of glacial acetic acid is added dropwise at room temperature over a period of three hours. The reaction is slightly exothermic. The reaction mixture is stirred at room temperature for another 3.5 hours. The precipitate is then filtered off with suction and the filtrate is admixed with 270 g of sodium acetate and concentrated. The residue is taken up in 2 l of dichloromethane and washed twice with 2 l of sodium bicarbonate solution and twice with sodium chloride solution. The organic phase is dried over sodium sulfate and concentrated.

後処理

  1. filtrationThe precipitate is then filtered off with suction
  2. concentrationconcentrated
  3. washwashed twice with 2 l of sodium bicarbonate solution and twice with sodium chloride solution
  4. dry with materialThe organic phase is dried over sodium sulfate
  5. concentrationconcentrated

出典と根拠

ORDレコード
ord-a87ccfffb570475bb5d1517393d2a26a
出典データセット
uspto-grants-2003_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06670482B2

反応ノート

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