Phenyl isocyanate → HCID 22761475, Verbindung

HRID 1703452Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1703452
[C:1]1([N:7]=[C:8]=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[N:10]1([CH2:16][C:17]2[CH:22]=[C:21]([CH3:23])[CH:20]=[C:19]([CH3:24])[C:18]=2[OH:25])[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]1>C1C=CC=CC=1>[N:10]1([CH2:16][C:17]2[CH:22]=[C:21]([CH3:23])[CH:20]=[C:19]([CH3:24])[C:18]=2[O:25][C:8](=[O:9])[NH:7][C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]1

Komponenten

4

Edukt 2

HCID 7672Phenyl isocyanateHCID 2626172,4-dimethyl-6-(piperidin-1-ylmethyl)phenol

Produkt 1

HCID 22761475HCID 22761475, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 241BenzeneLösungsmittel

Versuchsvorschrift

29.75 g (0.25 mol) of phenylisocyanate are introduced dropwise at 0° to 5° C. into a solution of 54.75g (0.25 mol) of 2-(piperidinomethyl)-4,6-dimethylphenol in 80 ml of anhydrous benzene. The reaction mixture is stirred at room temperature for 4 hours. The precipitated carbamic acid ester is suction filtered and washed with petroleum ether (b.p. 30°-50° C.).

Aufarbeitung

  1. filtrationfiltered
  2. washwashed with petroleum ether (b.p. 30°-50° C.)

Quellen und Nachweise

ORD-Eintrag
ord-c2b884e5648e46f2954bd7de8be3a7e7
Quelldatensatz
uspto-grants-1978_11
Patentnummer
US04124545

Notizen zur Reaktion

Wird geladen…