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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710226Generated: October 27, 2026

Salbutamol → [(1,1-Dimethylethyl)(phenylmethyl)-amino]acetyl-2-hydroxybenzoate

https://huagongshe.com/reaction/1710226

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalbutamolHCID 2083—
ReactantAcetophenoneHCID 7410—
ReactantN-(1,1-Dimethylethyl)benzenemethanamineHCID 76908—
ReactantBromoacetyl-2-hydroxybenzoateHCID 21684415—
Product[(1,1-Dimethylethyl)(phenylmethyl)-amino]acetyl-2-hydroxybenzoateHCID 86744191—

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 numberUS04952729
Source datasetuspto-grants-1990_08
ORD IDord-a7ee21119a7b4553868bb6ad80262184
Source noteuspto-grants-1990_08