Methylamine → N-Methyl-5-nitro-isophthalamic acid ethyl ester

HRID 241692Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 241692
[CH3:1][NH2:2].[CH2:3]([O:5][C:6](=[O:19])[C:7]1[CH:12]=[C:11]([N+:13]([O-:15])=[O:14])[CH:10]=[C:9]([C:16](Cl)=[O:17])[CH:8]=1)[CH3:4]>C1COCC1>[CH2:3]([O:5][C:6](=[O:19])[C:7]1[CH:12]=[C:11]([N+:13]([O-:15])=[O:14])[CH:10]=[C:9]([C:16]([NH:2][CH3:1])=[O:17])[CH:8]=1)[CH3:4]

Komponenten

4

Edukt 2

HCID 6329MethylamineHCID 3023043Ethyl 3-(chlorocarbonyl)-5-nitrobenzoate

Produkt 1

HCID 47099901N-Methyl-5-nitro-isophthalamic acid ethyl ester

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

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).

Aufarbeitung

  1. filtrationfiltered
  2. concentrationThe filtrate was concentrated in vacuum
  3. customthe solid recrystallised from diethyl ether

Quellen und Nachweise

ORD-Eintrag
ord-ad51d96f4e4149249f39d7a1f214a62e
Quelldatensatz
uspto-grants-2014_02
Patentnummer
US08653075B2

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