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2-Methylbenzothiazole → 2,3-Dimethyl-benzothiazolium p-toluenesulfonate

HRID 345192
ノート
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反応式

HRID 345192 の反応式
[CH3:1][C:2]1[S:3][C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[N:6]=1.[C:11]1(C)[C:12]([S:17]([O:20]C)(=[O:19])=[O:18])=[CH:13][CH:14]=[CH:15][CH:16]=1>CC(C)=O>[CH3:1][C:2]1[S:3][C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[N+:6]=1[CH3:11].[CH3:1][C:15]1[CH:14]=[CH:13][C:12]([S:17]([OH:20])(=[O:18])=[O:19])=[CH:11][CH:16]=1
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 84462-MethylbenzothiazoleHCID 90076Benzenesulfonic acid, 2-methyl-, methyl ester

生成物 1

HCID 867451362,3-Dimethyl-benzothiazolium p-toluenesulfonate

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

2-Methylbenzothiazole (74.6 pbw) and methyl toluenesulfonate (93.1 pbw) are mixed with one another and heated with stirring. At about 120° C. an exothermic reaction starts, in which the temperature of the mixture rises to 180° C. The solution is kept at this temperature for 10 minutes and then cautiously poured into 1000 pbw of acetone. The suspension obtained is stirred for one hour. The precipitate is removed by filtration with suction and washed with acetone. The powder obtained is dried in vacuo over phosphorus pentoxide.

後処理

  1. temperatureheated
  2. customAt about 120° C. an exothermic reaction
  3. customrises to 180° C
  4. customThe suspension obtained
  5. stirringis stirred for one hour
  6. customThe precipitate is removed by filtration with suction
  7. washwashed with acetone
  8. customThe powder obtained
  9. dry with materialis dried in vacuo over phosphorus pentoxide

出典と根拠

ORDレコード
ord-db8d7c18eeed4441a26245dfa29e02b0
出典データセット
uspto-grants-1991_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05055579

反応ノート

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