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Triethylamine → 3-[4-(2,4,6-Trimethylbenzenesulfonamido)benzenesulfonyl]acrylonitrile

HRID 267583
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HRID 267583 반응식
[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[C:4]([CH3:9])[C:3]=1[S:10](Cl)(=[O:12])=[O:11].[NH2:14][C:15]1[CH:20]=[CH:19][C:18]([S:21]([CH:24]=[CH:25][C:26]#[N:27])(=[O:23])=[O:22])=[CH:17][CH:16]=1.C(N(CC)CC)C>C(Cl)(Cl)Cl>[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[C:4]([CH3:9])[C:3]=1[S:10]([NH:14][C:15]1[CH:16]=[CH:17][C:18]([S:21]([CH:24]=[CH:25][C:26]#[N:27])(=[O:23])=[O:22])=[CH:19][CH:20]=1)(=[O:12])=[O:11]
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참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 130462-Mesitylenesulfonyl chlorideHCID 545613262-Cyanovinyl 4-aminophenyl sulfone

생성물 1

HCID 540421243-[4-(2,4,6-Trimethylbenzenesulfonamido)benzenesulfonyl]acrylonitrile

시약·촉매·용매 1

HCID 6212Chloroform용매2회

실험 절차

A solution of 6.6 g (0.03 mol) of 2,4,6-trimethylbenzenesulfonyl chloride in 50 ml chloroform is added at room temperature to a stirred slurry of 6.3 g (0.03 mol) of 3-(4-aminobenzenesulfonyl)acrylonitrile in 100 ml chloroform, the slurry additionally containing 4 ml (0.03 mol) triethylamine, portionwise over a five minute period. After 3 hours stirring the reaction mixture is filtered. The chloroform solution is thereafter washed with water, dilute hydrochloric acid, and water, in that order, separated from the water layer, dried over anhydrous magnesium sulfate and evaporated. The recovered 3-[4-(2,4,6-trimethylbenzenesulfonamido)benzenesulfonyl]acrylonitrile has the formula: ##SPC18##

후처리

  1. filtrationis filtered
  2. washThe chloroform solution is thereafter washed with water, dilute hydrochloric acid, and water, in that order
  3. customseparated from the water layer
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customevaporated

출처 및 근거

ORD 기록
ord-501b42157c7c48e993889e85ba5b34ea
출처 데이터셋
uspto-grants-1976_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03943154

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