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

HRID 345192
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반응식

HRID 345192 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 84462-MethylbenzothiazoleHCID 90076Benzenesulfonic acid, 2-methyl-, methyl ester

생성물 1

HCID 867451362,3-Dimethyl-benzothiazolium p-toluenesulfonate

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-db8d7c18eeed4441a26245dfa29e02b0
출처 데이터셋
uspto-grants-1991_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05055579

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