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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634803Generated: October 31, 2026

Water → 4-(4-Aminomethylbenzyl)-nitrobenzene

https://huagongshe.com/reaction/634803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriphenylphosphineHCID 11776—
Reactant4-(4-Azidomethylbenzyl)-nitrobenzeneHCID 21877004—
SolventTetrahydrofuranHCID 8028—
Product4-(4-Aminomethylbenzyl)-nitrobenzeneHCID 2187673179%

Reaction Steps

A solution of 4-(4-azidomethylbenzyl)-nitrobenzene (5.835 g) in tetrahydrofuran (175 mL) was treated with water (0.43 mL) and triphenylphosphine (6.45 g, 1.1 eg). The mixture was stirred at room temperature for 18 hours, and the solvent was evaporated. The residue was suspended in water, and suspension made acidic by the dropwise addition of hydrochloric acid to about pH 1, then extracted with diethyl ether (3×). The aqueous phase was made alkaline with 50% aqueous sodium hydroxide, extracted with dichloromethane (3×) to afford a crude brown oil (5.66 g). Chromatography on silica gel, eluting with dichloromethane/methanol/ammonium hydroxide, gave 4-(4-aminomethylbenzyl)-nitrobenzene (3.91 g, 79%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06184242B2
Source datasetuspto-grants-2001_02
ORD IDord-90ef25e612c14ebf903c89d99e69c80c
Source noteuspto-grants-2001_02