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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829772Generated: October 31, 2026

Benzyl Chloride → 3-(Benzyloxy)-4-bromoaniline

https://huagongshe.com/reaction/1829772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantSodiumHCID 5360545—
Reactant5-Amino-2-bromophenolHCID 10130284—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
Product3-(Benzyloxy)-4-bromoanilineHCID 14659501106.9%

Reaction Steps

To a solution of 5-amino-2-bromo-phenol (35.2 g, 0.187 mol) in N,N-dimethylformamide (350 mL) was added potassium tert-butoxide (22.9 g, 0.204 mol). After 15 min, benzyl chloride (25.5 mL, 0.222 mol) was added within 2 min. The reaction was stirred during 4h and then poured onto an aqueous solution of sodium hydrogenocarbonate and extracted with ethyl acetate. The combined organic phases were washed with brine and water then dried over sodium sulfate, filtered, and evaporated under vacuum. 55.6 g of the title compound were obtained. Black solid, ISP-MS: m/e=279.1 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07064134B2
Source datasetuspto-grants-2006_06
ORD IDord-1c880621c1db4172bd6836cd422c1ea6
Source noteuspto-grants-2006_06