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Benzoyl Peroxide → Methyl 3-bromomethyl-2-chloro-4-methylsulfonylbenzoate

HRID 322053
ノート
印刷プレビュー

反応式

HRID 322053 の反応式
[Cl:1][C:2]1[C:11]([CH3:12])=[C:10]([S:13]([CH3:16])(=[O:15])=[O:14])[CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5].[Br:17]N1C(=O)CCC1=O.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>C(Cl)(Cl)(Cl)Cl>[Br:17][CH2:12][C:11]1[C:2]([Cl:1])=[C:3]([CH:8]=[CH:9][C:10]=1[S:13]([CH3:16])(=[O:15])=[O:14])[C:4]([O:6][CH3:7])=[O:5]
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 7187Benzoyl PeroxideHCID 67184N-bromobutanimideHCID 15132838Methyl 2-chloro-3-methyl-4-methylsulfonylbenzoate

生成物 1

HCID 10969914Methyl 3-bromomethyl-2-chloro-4-methylsulfonylbenzoate

試薬・触媒・溶媒 1

HCID 5943Carbon Tetrachloride溶媒

実験手順

44.14 g (0.17 mol) of methyl 2-chloro-3-methyl-4-methylsulfonylbenzoate were dissolved in 600 ml of carbon tetrachloride and treated with 29.91 g (0.17 mol) of N-bromosuccinimide and 0.41 g of dibenzoyl peroxide. The mixture was then refluxed and illuminated with a 300 W lamp. The reaction mixture was filtered, the filtrate was concentrated and the residue was taken up in diethyl ether. The solution was treated with n-heptane, and the precipitated solid was filtered off with suction and dried.

後処理

  1. temperatureThe mixture was then refluxed
  2. customilluminated with a 300 W lamp
  3. filtrationThe reaction mixture was filtered
  4. concentrationthe filtrate was concentrated
  5. additionThe solution was treated with n-heptane
  6. filtrationthe precipitated solid was filtered off with suction
  7. customdried

出典と根拠

ORDレコード
ord-4986003685854b7eb52de08da8cc0a1b
出典データセット
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06211216B1

反応ノート

読み込み中…

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