Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096625Generated: November 4, 2026

3-Methoxypropylamine → 3-methoxy-N-(3-methoxypropyl)-2-nitroaniline

https://huagongshe.com/reaction/1096625

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxypropylamineHCID 1672—
Reactant1-Fluoro-3-methoxy-2-nitrobenzeneHCID 2782776—
SolventDimethylformamideHCID 6228—
Product3-methoxy-N-(3-methoxypropyl)-2-nitroanilineHCID 6678507280%

Reaction Conditions

Temperature-15 °C

Reaction Steps

Into a 25 mL round bottomed was added 1-fluoro-3-methoxy-2-nitrobenzene (500 mg, 2.92 mmol) and N,N-dimethylforamide (5.8 mL). The flask was cooled to −15° C. and 3-methoxypropylamine (313 mg, 3.5 mmol) in N,N-dimethylforamide (2.2 mL) was slowly added. The reaction was allowed to warm to room temperature overnight. Solvent was removed under vacuum and the residue was purified by column chromatography (20% ethylacetate:hexanes) to give 3-methoxy-N-(3-methoxypropyl)-2-nitroaniline (37A) as a yellow oil (560 mg, 80% yield). ESI-MS:m/z 241.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138168B1
Source datasetuspto-grants-2012_03
ORD IDord-d4e60868906449e39abb1a1a99a41b29
Source noteuspto-grants-2012_03