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Dabco → HCID 68140610, 화합물

HRID 267592
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HRID 267592 반응식
[C:1]1([CH3:10])[CH:6]=[CH:5][C:4]([S:7](Cl)=[O:8])=[CH:3][CH:2]=1.[NH2:11][C:12]1[CH:17]=[CH:16][C:15]([S:18]([CH:21]=[CH:22][C:23]#[N:24])(=[O:20])=[O:19])=[CH:14][CH:13]=1.N12CCN(CC1)CC2>CC(C)=O>[CH3:10][C:1]1[CH:6]=[CH:5][C:4]([S:7]([NH:11][C:12]2[CH:13]=[CH:14][C:15]([S:18]([CH:21]=[CH:22][C:23]#[N:24])(=[O:20])=[O:19])=[CH:16][CH:17]=2)=[O:8])=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 9237DabcoHCID 41900044-Methylbenzene-1-sulfinyl chlorideHCID 545613262-Cyanovinyl 4-aminophenyl sulfone

생성물 1

HCID 68140610HCID 68140610, 화합물

시약·촉매·용매 1

HCID 180Acetone용매3회

실험 절차

17.5 g p-toluenesulfinyl chloride (obtained by treating sodium toluenesulfinate.2H2O with thionyl chloride) is dissolved in 100 ml of acetone and this solution is added at room temperature and with stirring to a solution of 20.8 g (0.1 mol) of 2-cyanovinyl 4-aminophenyl sulfone in 250 ml of acetone. Shortly thereafter a solution of 11.2 g (0.1 mol) of 1,4-diazabicyclo[2.2.2]octane in 150 ml of acetone is added over about 10 minutes and the reaction mixture is stirred for another 20 minutes. The reaction mixture is filtered, evaporated in air to about a third of its volume, and then poured into cold water. The precipitate is filtered, washed and dried to give 3-[4-(4-methylbenzenesulfinamido)benzenesulfonyl]acrylonitrile: ##SPC45##

후처리

  1. additionthis solution is added at room temperature
  2. filtrationThe reaction mixture is filtered
  3. customevaporated in air to about a third of its volume
  4. additionpoured into cold water
  5. filtrationThe precipitate is filtered
  6. washwashed
  7. customdried

출처 및 근거

ORD 기록
ord-47a1697a1e5648b68c6e652a38023d48
출처 데이터셋
uspto-grants-1976_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03943154

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