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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085997Generated: October 25, 2026

Salbutamol → Methyl-5[[(1,1-dimethylethyl)(phenylmethyl)-amino]acetyl]-2-hydroxybenzoate

https://huagongshe.com/reaction/1085997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalbutamolHCID 2083—
ReactantAcetophenoneHCID 7410—
ReactantN-(1,1-Dimethylethyl)benzenemethanamineHCID 76908—
ReactantBromoacetyl-2-hydroxybenzoateHCID 21684415—
ProductMethyl-5[[(1,1-dimethylethyl)(phenylmethyl)-amino]acetyl]-2-hydroxybenzoateHCID 12814682—

Reaction Steps

Albuterol has been prepared, see Irish Patent Specification No. 31391, Aug. 9, 1972, starting from the appropriate acetophenone derivative methyl-5-(bromoacetyl-2-hydroxybenzoate, by condensation with N-(1,1-dimethylethyl)benzenemethanamine in the presence of base to form the ketonic ester, methyl-5[[(1,1-dimethylethyl)(phenylmethyl)-amino]acetyl]-2-hydroxybenzoate. The ketonic ester is reduced with lithium aluminum hydride in tetrahydrofuran under nitrogen to yield α1 -[[(1,1-dimethylethyl)-(phenylmethyl)amino]methyl]-4-hydroxy-1,3-benzenedimethanol which is subsequently debenzylated with hydrogen in the presence of palladium on carbon catalyst to produce albuterol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05011993
Source datasetuspto-grants-1991_04
ORD IDord-5b8dcbadf97f4773909981ee451ff8e5
Source noteuspto-grants-1991_04