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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119334Generated: November 1, 2026

Methylamine → N-methyl-5-(morpholin-4-ylmethyl)-2-nitroaniline

https://huagongshe.com/reaction/2119334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant4-(3-FLUORO-4-NITROBENZYL)MORPHOLINEHCID 11276495—
SolventDimethyl SulfoxideHCID 679—
ProductN-methyl-5-(morpholin-4-ylmethyl)-2-nitroanilineHCID 23441210—

Reaction Conditions

Temperature47 °C

Reaction Steps

An aqueous solution of methylamine (40 wt %, 910 ml) at 30° C. is added to a 61° C. solution of 4-(3-fluoro-4-nitrobenzyl)morpholine (504 g) in DMSO (810 ml) followed by a DMSO rinse (150 ml) over ½ h. The mixture is allowed to reflux at 47 ° C. over 5 min then maintained at <51° C. by occasional ice bath cooling for remainder of the addition. The mixture is stirred at 50° C. for ¾ h and then water (2000 ml) is added. The mixture is cooled to 0° C. and the precipitate is collected by filtration, washed with water (1500 ml) and is dried in a nitrogen stream to give a bright orange solid (529 g). Physical characteristics: 1H NMR (400 MHz, DMSO-d6) δ2.35, 2.93, 3.44, 3.56, 6.63, 6.64, 7.78, 8.15; 13C NMR (100 MHz, DMSO-d6) δ29.95, 53.57, 62.27,66.54, 113.69, 115.76, 126.49, 130.16, 146.27, 148.07.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06686356B2
Source datasetuspto-grants-2004_02
ORD IDord-6da8db1285e74a26b75f9921d8c86fe4
Source noteuspto-grants-2004_02