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Toluene → HCID 20535994, 화합물

HRID 1075495
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HRID 1075495 반응식
Cl[CH2:2][CH2:3][S:4]([C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([N+:13]([O-:15])=[O:14])[CH:8]=1)(=[O:6])=[O:5].C1(C)C=CC=CC=1.C(=O)([O-])[O-].[K+].[K+]>C(N(CC)CC)C.O>[N+:13]([C:9]1[CH:8]=[C:7]([S:4]([CH:3]=[CH2:2])(=[O:6])=[O:5])[CH:12]=[CH:11][CH:10]=1)([O-:15])=[O:14]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 1140TolueneHCID 11430Potassium CarbonateHCID 434616951-(beta-Chloroethylsulfonyl)-3-nitrobenzene

생성물 1

HCID 20535994HCID 20535994, 화합물수율 94.3%

시약·촉매·용매 2

HCID 8471Triethylamine촉매HCID 962Water용매

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온도
40 °C

실험 절차

1-(β-chloroethylsulfonyl)-3-nitrobenzene (2.50 g, 10 mmol) was added to 20 g of toluene, to this solution were added 1.50 g of 49% aqueous potassium carbonate solution (potassium carbonate 5.3 mmol) and 50 mg (0.5 mmol) of triethylamine, and the mixture was stirred for 2 hours at 40° C. Then, 10 g of water was added and the mixture was separated to an organic phase and aqueous phase. This aqueous phase was extracted by chloroform, and the resulted organic phase was combined with the previous organic phase, dried over magnesium sulfate, the solvents were distilled off, to obtain 2.00 g (yield 94.3%) of (3-nitrophenyl)vinylsulfone.

후처리

  1. customthe mixture was separated to an organic phase and aqueous phase
  2. extractionThis aqueous phase was extracted by chloroform
  3. dry with materialdried over magnesium sulfate
  4. distillationthe solvents were distilled off

출처 및 근거

ORD 기록
ord-3d29567437e34bdcbf7054ae5276ff58
출처 데이터셋
uspto-grants-1999_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05902905

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