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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548238Generated: October 29, 2026

Ammonia → 3-Nitrobenzylamine

https://huagongshe.com/reaction/548238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantBenzene, 1-(bromomethyl)-3-nitro-HCID 77568—
SolventEthanolHCID 702—
Product3-NitrobenzylamineHCID 12272265%

Reaction Steps

3-Nitrobenzyl bromide (10 g, 46.3 mmol) was dissolved in ethanol (200 ml) and stirred at room temperature A solution of conc. NH3 (aq) (200 ml) in ethanol (300 ml) was added dropwise to the reaction over 30 minutes. The reaction was stirred for 18 h at room temperature before evaporating to dryness. Water (350 ml) was added to the residue and the solution was washed with EtOAc (2×200 ml). The aqueous layer was basified with 1M NaOH and extracted with EtOAc (2×200 ml). The organic extracts of the basic layer were combined, dried (Na2SO4) and evaporated to dryness. The product was obtained as an orange oil (4.6 g, 65% yield). LCMS purity 100%, m/z 153 [M++H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07939666B2
Source datasetuspto-grants-2011_05
ORD IDord-1806e3f6cd964b07980622ad6f87ff27
Source noteuspto-grants-2011_05