تفاعل #1509590

ord-e13cc62fd39e4d038af6210ca3511aa9

معادلة التفاعل

CN
methylamine
CCOC(=O)c1cc(C(=O)Cl)cc([N+](=O)[O-])c1
3-chlorocarbonyl-5-nitro-benzoic acid ethyl ester
CCOC(=O)c1cc(C(=O)NC)cc([N+](=O)[O-])c1
title compound
CCOC(=O)c1cc(C(=O)NC)cc([N+](=O)[O-])c1
N-Methyl-5-nitro-isophthalamic acid ethyl ester

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحfiltered
  2. 2
    تركيزThe filtrate was concentrated in vacuum
  3. 3
    أخرىthe solid recrystallised from diethyl ether

الإجراء التجريبي

To a 2M solution of methylamine in THF (256 ml) at −20° C. was added a pre-cooled solution of 3-chlorocarbonyl-5-nitro-benzoic acid ethyl ester (60 g) in THF (500 ml) dropwise. This was stirred for 20 min and then filtered. The filtrate was concentrated in vacuum and the solid recrystallised from diethyl ether to give the title compound (22.5 g) as a solid. An oxalyl chloride solution in DCM (63 ml, 2M), was added with DMF (5 ml). The reaction was stirred for 2 h and then concentrated in vacuum. The residue was triturated with toluene and again concentrated in vacuum leaving the title compound (60 g). Rt=1.53 min (method D).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: USRE045323E1uspto-grants-2015_01