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Ethyl p-methylbenzenesulfonate → 3-Ethyl-2-(ethylsulfanyl)-1,3-benzothiazol-3-ium 4-methylbenzene-1-sulfonate

HRID 223755
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인쇄 미리보기

반응식

HRID 223755 반응식
S[C:2]1[S:3][C:4]2[CH:10]=CC=[CH:7][C:5]=2[N:6]=1.[C:11]1([CH3:23])[CH:16]=[CH:15][C:14]([S:17]([O:20]CC)(=[O:19])=[O:18])=[CH:13][CH:12]=1>C(O)C>[C:11]1([CH3:23])[CH:12]=[CH:13][C:14]([S:17]([O-:20])(=[O:18])=[O:19])=[CH:15][CH:16]=1.[CH2:4]([S:3][C:2]1[S:17][C:14]2[CH:13]=[CH:12][CH:11]=[CH:16][C:15]=2[N+:6]=1[CH2:5][CH3:7])[CH3:10]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6638Ethyl p-methylbenzenesulfonateHCID 178418395HCID 178418395, 화합물

생성물 1

HCID 140905473-Ethyl-2-(ethylsulfanyl)-1,3-benzothiazol-3-ium 4-methylbenzene-1-sulfonate

시약·촉매·용매 1

HCID 702Ethanol용매2회

반응 조건

온도
150 °C

실험 절차

A mixture of 3.3 g of 2-mercaptobenzothiazole and 10.0 g of ethyl p-toluenesulfonate was heated to 150° C. to react them for 6 hours. The reaction product was cooled to 80° C. and then 30 ml of ethanol was added to it, thereby producing an ethanol solution of 2-ethylmercapto-3-ethylbenzothiazolium p-toluenesulfonate.

후처리

  1. customto react them for 6 hours
  2. temperatureThe reaction product was cooled to 80° C.

출처 및 근거

ORD 기록
ord-fab06d8802f34d2882e5fc578177755c
출처 데이터셋
uspto-grants-1982_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04356247

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