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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375455Generated: November 1, 2026

Benzyl Chloride → 4-Benzyloxy-3-chloroaniline

https://huagongshe.com/reaction/1375455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium HydroxideHCID 14797—
Reactant4-Amino-2-chlorophenolHCID 77578—
CatalystTetrabutylammonium BromideHCID 74236—
SolventAcetoneHCID 180—
Product4-Benzyloxy-3-chloroanilineHCID 126828580%

Reaction Steps

To 4-amino-2-chlorophenol (7.23 g, 50 mmol) dissolved in acetone (250 mL), was added potassium carbonate (6.94 g, 50 mmol), followed by the addition of benzyl chloride (5.8 mL, 50 mmol), tetrabutylammonium bromide (TBAB) (1.66 g, 5 mmol), and potassium hydroxide (2.84 g, 50 mmol). The reaction mixture was allowed to stir at reflux overnight under nitrogen. The reaction mixture was extracted three times using dichloromethane; the combined organic layers were washed with brine and dried over potassium carbonate. The sample was concentrated and the resulting oil was dried overnight under vacuum. The material was purified by silica gel flash column chromatography eluting with 50:50 v:v hexanes:ethyl acetate and the collected fractions were concentrated in vacuo to give E1 (9.3 g, 80%); mp 54° C.; HPLC: Inertsil ODS 3V C18, 40:30:30 [KH2PO4 (0.01 M, pH 3.2): CH3OH:CH3CN], 264 nm, Rt 14.8 min, 98.7% purity; MS (TOF ES+) m/z 234 (M+H, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169784B2
Source datasetuspto-grants-2007_01
ORD IDord-06de4e08a0824c829db127ef37ba9fe5
Source noteuspto-grants-2007_01