Réaction #2383802

ord-e8fb9aff2ab645e2956e7959a07f33f8

Équation de réaction

[Na+].[OH-]
sodium hydroxide
Cl.O=[N+]([O-])c1ccc2c(c1)CNCCO2
7-nitro-2,3,4,5-tetrahydro-1,4-benzoxazepine hydrochloride
C=O
formaldehyde
O=CO
formic acid
CN1CCOc2ccc([N+](=O)[O-])cc2C1.Cl
solid
Rendement 61.5%
CN1CCOc2ccc([N+](=O)[O-])cc2C1.Cl
4-Methyl-7-nitro-2,3,4,5-tetrahydro-1,4-benzoxazepine hydrochloride
Rendement 61.5%

Solvants

Conditions de réaction

Température
80°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurecooled

Mode opératoire

A mixture of 7-nitro-2,3,4,5-tetrahydro-1,4-benzoxazepine hydrochloride (11.53 g, 50 mmol), 37% formaldehyde (25 ml, 335 mmol) and 88% formic acid (15 ml, 340 mmol) was heated at 80° C. for 24 h, cooled and poured into water (150 ml). The suspension was Is basified with 25% aqueous sodium hydroxide to give a brown solid (7.52 g). The aqueous layer was extracted with methylene chloride (3×200 ml), washed with saturated brine solution, and dried over magnesium sulphate to give yellow crystals (1.02 g). This sample was combined with the solid obtained earlier and suspended in isopropanol (750 ml), refluxed for several hours and then filtered. The filtrate was acidified to give the title compound (9.51 g).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US06489322B1uspto-grants-2002_12