Reacción #792177

ord-eacde490872e41f79fb7543f794a4a31

Ecuación de reacción

Cc1cc(Cl)cc(C(=O)O)c1N
2-amino-3-methyl-5-chlorobenzoic acid
Cc1cc(Cl)cc(C(=O)O)c1N
2-Amino-3-methyl-5-chlorobenzoic acid
Cc1cc(Cl)cc(C(=O)O)c1N
product
Cc1cc(Cl)cc(C(=O)O)c1N
2-Amino-3-methyl-5-chlorobenzoic acid
O=C(Cl)OC(Cl)(Cl)Cl
trichloromethyl chloroformate
Cc1cc(Cl)cc2c(=O)oc(=O)[nH]c12
title compound
Cc1cc(Cl)cc2c(=O)oc(=O)[nH]c12
6-Chloro-8-methyl-2H-3,1-benzoxazine-2,4(1H)-dione

Disolventes

Condiciones de reacción

Temperatura
42°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.DISSOLUTIONthe solid almost completely dissolved before a thick suspension
  2. 2
    Otroformed again

Procedimiento

To a suspension of 2-amino-3-methyl-5-chlorobenzoic acid (i.e. product of Example 6, Step A) (97 g, 520 mmol) stirred in dry dioxane (750 mL) at room temperature, trichloromethyl chloroformate (63 g, 320 mmol) was added dropwise. The reaction mixture exothermically warmed slowly to 42° C., and the solid almost completely dissolved before a thick suspension formed again. After the suspension was stirred at ambient temperature for 2.5 hours, the title compound was isolated by filtration, washed with ethyl ether, and dried to yield the title product compound, obtained as a white solid (98 g).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09173400B2uspto-grants-2015_11