Triethylamine → (E)-N-(4'-chlorobiphenyl-4-yl)-3-(4-chloromethylphenyl)acrylamide

HRID 735172Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 735172
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][C:11]([NH:14][C:15](=[O:26])/[CH:16]=[CH:17]/[C:18]3[CH:23]=[CH:22][C:21]([CH2:24]O)=[CH:20][CH:19]=3)=[CH:10][CH:9]=2)=[CH:4][CH:3]=1.C(N(CC)CC)C.CS([Cl:38])(=O)=O>ClCCl.O>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][C:11]([NH:14][C:15](=[O:26])/[CH:16]=[CH:17]/[C:18]3[CH:23]=[CH:22][C:21]([CH2:24][Cl:38])=[CH:20][CH:19]=3)=[CH:10][CH:9]=2)=[CH:4][CH:3]=1

Komponenten

6

Versuchsvorschrift

A suspension of 2.1 g (5.77 mmol) of (E)-N-(4′-chlorobiphenyl-4-yl)-3-(4-hydroxymethylphenyl)acrylamide in 100 mL of dichloromethane is combined with 1.7 mL (12.19 mmol) of triethylamine and then combined with 0.46 mL (5.88 mmol) of methanesulfonic acid chloride. The reaction mixture is stirred for 3 hours at ambient temperature, diluted with water, and extracted several times with dichloromethane. The combined organic phases are dried over sodium sulfate, filtered through silica gel, and the filtrate is evaporated down. Yield: 0.4 g (18.1% of theory); C22H17Cl2NO (M=382.29); calc.: molecular ion peak (M+H)+: 381/383/385; found: molecular ion peak (M+H)+: 381/383/385.

Aufarbeitung

  1. extractionextracted several times with dichloromethane
  2. dry with materialThe combined organic phases are dried over sodium sulfate
  3. filtrationfiltered through silica gel
  4. customthe filtrate is evaporated down

Quellen und Nachweise

ORD-Eintrag
ord-f8b38b86834c44ed9354a5f963b8867a
Quelldatensatz
uspto-grants-2009_09
Patentnummer
US07592373B2

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