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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384352Generated: October 29, 2026

Methanol → 4-(3-Amino-2-hydroxy-phenyl)-furan-2-carboxylic acid hydrobromide

https://huagongshe.com/reaction/384352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBoron tribromideHCID 25134—
Reactant4-(3-Amino-2-methoxy-phenyl)-furan-2-carboxylic acidHCID 57483825—
SolventDichloromethaneHCID 6344—
Product4-(3-Amino-2-hydroxy-phenyl)-furan-2-carboxylic acid hydrobromideHCID 5748382657.1%

Reaction Steps

4-(3-Amino-2-methoxy-phenyl)-furan-2-carboxylic acid 28d (325 mg, 1.4 mmol) was dissolved in 5 mL of dichloromethane followed by dropwise addition of boron tribromide (2.8 mL, 5.6 mmol). The mixture was reacted at room temperature for 4.5 hours. The reaction was monitored by TLC until the disappearance of the starting materials. 5 mL of methanol was added and then the mixture was concentrated under reduced pressure. The residue was diluted with 10 mL of ethyl acetate and stirred for 0.5 hours. The mixture was filtered and the filter cake was dried to obtain the title compound 4-(3-amino-2-hydroxy-phenyl)-furan-2-carboxylic acid hydrobromide 28e (174 mg, yield 57.1%) as a grey solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367710B2
Source datasetuspto-grants-2013_02
ORD IDord-a6090cf75ec145898344e9e4ffb8e387
Source noteuspto-grants-2013_02