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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110242Generated: November 4, 2026

Methanol → Methyl 4-{[(2-hydroxyphenethyl)amino]methyl}benzoate

https://huagongshe.com/reaction/2110242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBoron tribromideHCID 25134—
ReactantMethyl 4-(((2-methoxyphenethyl)amino)methyl)benzoateHCID 11231852—
SolventDichloromethaneHCID 6344—
ProductMethyl 4-{[(2-hydroxyphenethyl)amino]methyl}benzoateHCID 11233903—

Reaction Conditions

Temperature0 °C

Reaction Steps

At 0° C., 176.8 ml (176.8 mmol) of a 1N boron tribromide solution in methylene chloride are added dropwise to 16.03 g (53.561 mmol) of methyl 4-{[(2-methoxyphenethyl)amino]methyl}benzoate from Example. I.1 in 100 ml of methylene chloride. After one hour of stirring at 0° C., 150 ml of methanol are added and the solution is heated at reflux for 4 hours. The solvent is distilled off under reduced pressure and the residue is taken up in a mixture of 190 ml of ethyl acetate and 10 ml of methanol. Using 10% strength sodium carbonate solution, the mixture is made alkaline and extracted with ethyl acetate/methanol 9/1. The combined organic phases are washed with saturated sodium chloride solution and dried over magnesium sulphate, and the solvent is distilled off under reduced pressure. The crude product is purified by chromatography over silica gel (0.04-0.063 nm) using the mobile phase methylene chloride/methanol 100/2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517896B2
Source datasetuspto-grants-2009_04
ORD IDord-c36f65aad7ef47d9ac9250eca8f6e2ed
Source noteuspto-grants-2009_04