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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301061Generated: November 1, 2026

2-Chloro-4-benzylnitrobenzene → 2-Chloro-4-benzylaniline

https://huagongshe.com/reaction/2301061

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-4-benzylnitrobenzeneHCID 22287159—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product2-Chloro-4-benzylanilineHCID 2228734544.9%

Reaction Steps

A solution of 2-chloro-4-benzylnitrobenzene (Method 29) (0.60 g) in ethyl acetate was treated with 10% Pd/C (0.06 g) under argon. The mixture was then stirred under a hydrogen atmosphere for 10 hours. The mixture was filtered under argon and extracted with aqueous hydrochloric acid (50% v/v, 50 ml). The aqueous layer was separated, basified with 2M aqueous NaOH and extracted with ethyl acetate to give the title compound as an oil (0.237 g). NMR: 3.6 (s, 2H), 5.1 (brs, 2H), 6.7 (d, 1H), 6.9 (dd, 1H), 7.0(d, 1H), 7.1-7.3 (m, 5H), MS (CI): 218 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498275B1
Source datasetuspto-grants-2002_12
ORD IDord-c2ce37d68ef641f2b6b6b956091f8eab
Source noteuspto-grants-2002_12