Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261837Generated: November 3, 2026

Hydrochloric Acid → 4-{[(2-Fluoro-4-hydroxy-6-methyl-phenyl)-methyl-amino]-methyl}-2-methyl-benzoic acid methyl ester

https://huagongshe.com/reaction/2261837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant4-{[(2-Fluoro-6-methyl-4-triisopropylsilanyloxy-phenyl)-methyl-amino]-methyl}-2-methyl-benzoic acid methyl esterHCID 57443349—
SolventTetrahydrofuranHCID 8028—
Product4-{[(2-Fluoro-4-hydroxy-6-methyl-phenyl)-methyl-amino]-methyl}-2-methyl-benzoic acid methyl esterHCID 6752806476.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 4-{[(2-fluoro-6-methyl-4-triisopropylsilanyloxy-phenyl)-methyl-amino]-methyl}-2-methyl-benzoic acid methyl ester (457 mg, 0.965 mmol) and tetrabutylammonium fluoride (2.0 mL of 1M in THF, 2.0 mmol) in THF (10 mL) is stirred at 0° C. for 20 minutes and then 2.0 mL of 1M HCl is added and the mixture is concentrated. The residue is portioned between ethyl acetate and brine. The layers are separated and the brine layer is extracted with ethyl acetate. The combined ethyl acetate layers are dried (MgSO4) and concentrated. The residue is purified on 40 g silica with ethyl acetate in heptane gradient (10% to 70%) to provide 233 mg (76%) of the titled compound as a glass. LC-ES/MS m/e 318.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846960B2
Source datasetuspto-grants-2010_12
ORD IDord-f2758d59b18d41259792b9ea7dad92b1
Source noteuspto-grants-2010_12