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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238716Generated: October 30, 2026

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

https://huagongshe.com/reaction/238716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBoron tribromideHCID 25134—
Reactant4-(3-Amino-2-methoxy-phenyl)-thiophene-2-carboxylic acid hydrobromideHCID 57483848—
SolventDichloromethaneHCID 6344—
Product4-(3-Amino-2-hydroxy-phenyl)-thiophene-2-carboxylic acid hydrobromideHCID 5748384617.5%

Reaction Steps

4-(3-Amino-2-methoxy-phenyl)-thiophene-2-carboxylic acid hydrobromide 19b (360 mg, 1.45 mmol) was dissolved in 5 mL of dichloromethane followed by dropwise addition of boron tribromide (2.8 mL, 5.6 mmol). The reaction mixture was reacted at room temperature for 4.5 hours. The reaction mixture was added with 5 mL of methanol and 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)-thiophene-2-carboxylic acid hydrobromide 19c (80 mg, yield 17.5%) as a grey solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642637B2
Source datasetuspto-grants-2014_02
ORD IDord-ebac0666daf9434a81a06d62d0848ec7
Source noteuspto-grants-2014_02