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Chlorine → 4,5-Dichloro-2-methyl-4-isothiazolin-3-one

HRID 426526
ノート
印刷プレビュー

反応式

HRID 426526 の反応式
[ClH:1].[CH3:2][N:3]1[C:7](=[O:8])[CH:6]=[CH:5][S:4]1.[Cl:9]Cl>C(OCC)(=O)C>[Cl:1][C:6]1[C:7](=[O:8])[N:3]([CH3:2])[S:4][C:5]=1[Cl:9]
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 24526ChlorineHCID 1177462-Methyl-4-isothiazolin-3-one hydrochloride

生成物 1

HCID 1470174,5-Dichloro-2-methyl-4-isothiazolin-3-one

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

実験手順

To a suspension of 30.3 g (0.2 mole) of pure and dry 2-methyl-4-isothiazolin-3-one hydrochloride in 200 ml. of ethyl acetate is added over 1 hour, 71 g (1 mole) of chlorine. The reaction exotherms to 55° C. in 1/2 hour and all solid is dissolved after about 3/4 hour. The solution is degassed and evaporated under reduced pressure to give a cream color mush. The mush is shown by TLC (silica/toluene) to contain two major components. Crystallization of the mush from methanol gives 16.8 g of 4,5-dichloro-2-methyl-4-isothiazolin-3-one. Evaporation of the filtrate gives 23.4 of material which is chromatographed on a silica dry column with toluene. The fraction close to the solvent front is extracted and gives 8.8 g of crude product. Recrystallization from methanol gives 6.55 g (13% of white crystalline 2-methyl-4,4,5,5-tetrachloroisothiazolidin-3-one, m.p. 77°-80° C.

後処理

  1. dissolutionall solid is dissolved after about 3/4 hour
  2. customThe solution is degassed
  3. customevaporated under reduced pressure
  4. customto give a cream color mush
  5. customCrystallization of the mush from methanol

出典と根拠

ORDレコード
ord-fc2892e85bec4756be45540038963f06
出典データセット
uspto-grants-1979_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04169949

反応ノート

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