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Water → 2-(Benzylthio)benzo[d]thiazole

HRID 1590165
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HRID 1590165 반응식
[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[SH:10].C(N(CC)CC)C.[CH2:18](Br)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.O>CN(C)C=O>[CH2:18]([S:10][C:2]1[S:1][C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=1)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 7498Benzyl BromideHCID 8471TriethylamineHCID 178418395HCID 178418395, 화합물

생성물 1

HCID 4974652-(Benzylthio)benzo[d]thiazole

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

실험 절차

To a solution of 2-benzothiazolthiol (250 g) in N,N-dimethylformamide (1 l) was added triethylamine (208 ml) under ice-cooling and dropwise a solution of benzyl bromide (178 ml) in N,N-dimethylformamide (300 ml) and the mixture was stirred for 40 minutes. The resulting solution was poured into water (10 l) and the formed precipitate was separated by filtration and dissolved in dichloromethane (3 l). After drying over anhydorous magnesium sulfate, dichloromethane was removed in vacuo to give 378 g of the objective compound.

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후처리

  1. temperaturecooling
  2. customthe formed precipitate was separated by filtration
  3. dissolutiondissolved in dichloromethane (3 l)
  4. dry with materialAfter drying over anhydorous magnesium sulfate, dichloromethane
  5. customwas removed in vacuo

출처 및 근거

ORD 기록
ord-d8fc01cac543427cb507baee2651e475
출처 데이터셋
uspto-grants-1993_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05202339

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