Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475316Generated: October 30, 2026

Ethanol → (2-Amino-5-bromo-3-methoxyphenyl)methanol

https://huagongshe.com/reaction/475316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
Reactant2-Amino-5-bromo-3-methoxybenzoic acidHCID 45480457—
SolventTetrahydrofuranHCID 8028—
Product(2-Amino-5-bromo-3-methoxyphenyl)methanolHCID 46738297—

Reaction Conditions

Temperature0 °C

Reaction Steps

2-amino-5-bromo-3-methoxybenzoic acid (20.0 g, 81.30 mmol) is suspended in 250 mL THF, cooled to 0° C. and combined with borane-THF complex (315 mL, 0.315 mol). The reaction mixture is stirred for 5 d at 20° C. and then combined with 10 mL EtOH, stirred for 15 min and then stirred into 250 mL water. The mixture is extracted 3× with DCM, the combined organic phases are dried and the solvent is eliminated in vacuo. The crude product is suspended in DCM and extracted 2× with 400 mL 1 N hydrochloric acid. The combined aqueous phases are adjusted to pH 5-6 with potassium carbonate, the precipitate formed is filtered off and (2-amino-5-bromo-3-methoxy-phenyl)-methanol (HPLC-MS: tRet.=1.41 min, MS(M+H)+=232/234; method FEC3) is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637549B2
Source datasetuspto-grants-2014_01
ORD IDord-1d642fcfe5fa48daa9ad3998695a57e1
Source noteuspto-grants-2014_01