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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743932Generated: October 30, 2026

Boron Trichloride → 5-Amino-2-bromophenol

https://huagongshe.com/reaction/1743932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron TrichlorideHCID 25135—
Reactant4-Bromo-3-methoxyanilineHCID 7018254—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDichloromethaneHCID 6344—
Product5-Amino-2-bromophenolHCID 10130284100.7%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A suspension of 4-bromo-3-methoxy-phenylamine (37.6 g, 0.186 mol) and tetrabutylammonium iodide (96 g, 0.260 mol) in dichloromethane (1.2 L) was cooled down to −78° C. A 1M solution of boron trichloride in dichloromethane (520 mL, 0.521 mol) was added dropwise, within 20 min. The cooling bath was removed. After 3 hours, the reaction mixture was poured onto ice water (4.5 kg). The organic layer was extracted with water. The combined aqueous layers were washed with dichloromethane. The pH was adjusted to 9 using sodium hydrogencarbonate. Sodium chloride was added until saturation. The aqueous layer was extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate, filtered and the solvents were evaporated. The solid was washed with dichloromethane and dried under vacuum. 35.2 g of the title compound were obtained. Brown solid, ISP-MS: m/e=189.1 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07012073B2
Source datasetuspto-grants-2006_03
ORD IDord-1331a5d9aba04e0f91018df19b8f30e4
Source noteuspto-grants-2006_03