Phosphorus pentachloride → 4-chloro-2,2-dimethyl-3H-1,3-benzoxazine

HRID 381255

Reaktionsgleichung

Reaktionsgleichung von HRID 381255
[CH3:1][C:2]1([CH3:13])[NH:7][C:6](=O)[C:5]2[CH:9]=[CH:10][CH:11]=[CH:12][C:4]=2[O:3]1.P(Cl)(Cl)(Cl)(Cl)[Cl:15]>O=P(Cl)(Cl)Cl>[Cl:15][CH:6]1[C:5]2[CH:9]=[CH:10][CH:11]=[CH:12][C:4]=2[O:3][C:2]([CH3:13])([CH3:1])[NH:7]1

Komponenten

4

Edukt 2

HCID 24819Phosphorus pentachlorideHCID 7174282,2-dimethyl-3,4-dihydro-2H-1,3-benzoxazin-4-one

Produkt 1

HCID 222447204-chloro-2,2-dimethyl-3H-1,3-benzoxazine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 24813Phosphorus oxychlorideLösungsmittel

Versuchsvorschrift

A solution of 2,2-dimethyl-4-keto-1,3-benzoxazine (1.77 g, 10.0 mmol) and PCl5 (2.09 g, 10.0 mmol) in POCl3 (3.0 mL) was stirred at RT for 1 h then at 50-60° C. for 2 h. The reaction was concentrated and the product distilled (90-95° C./2-3 mm Hg) to afford 4-chloro-2,2-dimethyl-3H-1,3-benzoxazine. (0.496 g, 25%) as a clear oil: 1H NMR (CDCl3, 300 MHz, ppm) 7.58 (d, 1H), 7.48 (m, 1H), 6.97 (m, 1H), 6.94 (d, 1H), 1.63 (s, 6H).

Aufarbeitung

  1. concentrationThe reaction was concentrated
  2. distillationthe product distilled (90-95° C./2-3 mm Hg)

Quellen und Nachweise

ORD-Eintrag
ord-ead02719994342e38f90758e4574baa7
Quelldatensatz
uspto-grants-2001_10
Patentnummer
US06306840B1

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