Triethylamine → 3-[(4-Dodecylbenzenesulfonamido)benzenesulfonyl]acrylonitrile

HRID 267582Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 267582
[CH2:1]([C:13]1[CH:18]=[CH:17][C:16]([S:19](Cl)(=[O:21])=[O:20])=[CH:15][CH:14]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].N[C:24]1[CH:29]=[CH:28][C:27]([S:30]([CH:33]=[CH:34][C:35]#[N:36])(=[O:32])=[O:31])=[CH:26][CH:25]=1.C([N:39](CC)CC)C>C([O-])(=O)C.CC(C)=O>[CH2:1]([C:13]1[CH:18]=[CH:17][C:16]([S:19]([NH:39][C:28]2[CH:29]=[CH:24][CH:25]=[CH:26][C:27]=2[S:30]([CH:33]=[CH:34][C:35]#[N:36])(=[O:32])=[O:31])(=[O:21])=[O:20])=[CH:15][CH:14]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]

Komponenten

6

Versuchsvorschrift

6.9 grams (0.02 mol) of 4-dodecylbenzenesulfonyl chloride dissolved in 100 ml acetate are added, at room temperature, to a stirred solution of 3-(4-aminobenzenesulfonyl)acrylonitrile (4.2 g, 0.02 mol) and 3ml (0.02 mol) of triethylamine in 150 ml acetone. The mixture is permitted to stand overnight. 3-[(4-dodecylbenzenesulfonamido)benzenesulfonyl]acrylonitrile is recovered as a soft, fine yellow powder: ##SPC17##

Aufarbeitung

  1. custom3-[(4-dodecylbenzenesulfonamido)benzenesulfonyl]acrylonitrile is recovered as a soft, fine yellow powder

Quellen und Nachweise

ORD-Eintrag
ord-e4f273a4111441fd921c2da30d7bc713
Quelldatensatz
uspto-grants-1976_03
Patentnummer
US03943154

Notizen zur Reaktion

Wird geladen…