Réaction #792177

ord-eacde490872e41f79fb7543f794a4a31

Équation de réaction

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

Solvants

Conditions de réaction

Température
42°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

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

Mode opératoire

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).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09173400B2uspto-grants-2015_11