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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610046Generated: October 25, 2026

Atenolol → Esatenolol

https://huagongshe.com/reaction/1610046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAtenololHCID 2249—
ReactantIsopropylamineHCID 6363—
ReactantDiglycidyl etherHCID 16704—
ProductEsatenololHCID 175540—

Reaction Steps

In order to prevent the reaction of produced atenolol with the optically active glycidyl ether (4) it is preferable to add the optically active glycidyl ether (4) to isopropyl amine in a solvent. The removal of excess isopropyl amine by distillation gave desired (S)-atenolol (1). Preferably, the distillation is carried out at atmospheric pressure at the initial stages and under reduced pressure at later stages, keeping the reaction mass temperature below 60° to 70° C., through out the distillation process. The crude residue may be purified, if required, by dissolving it in 1N HCl, treating this solution with activated charcoal, filtering the charcoal followed by treatment of alkali to precipitate the product. Thus, the solid product was isolated by conventional method such as filtration to get (S)-atenolol (1) of optical purity of 98% ee and above. If, necessary, the optically active (S)-atenolol (1) may be crystallized from an appropriate solvent such as water, alcohols, such as methanol, ethanol, isopropyl alcohol, butanol etc., ethers, such as diethyl ether, methyl tbutyl ether, diisopropyl ether or ketones, such as acetone, ethyl methyl ketone, methyl isobutyl ketone etc.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982349B1
Source datasetuspto-grants-2006_01
ORD IDord-e2324558f6104b96bacdaf691ac0074a
Source noteuspto-grants-2006_01