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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440052Generated: November 1, 2026

Hydrochloric Acid → methyl (3S)-3-amino-2-hydroxybutanoate

https://huagongshe.com/reaction/1440052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantTriethylamineHCID 8471—
Reactant(3S)-3-amino-2-hydroxybutanoic acidHCID 14058970—
SolventMethanolHCID 887—
Productmethyl (3S)-3-amino-2-hydroxybutanoateHCID 56623301—

Reaction Steps

Into a suspension of (3S)-3-amino-2-hydroxybutanoic acid (1.0 g, 8.4 mmol) in methanol (25 ml) was bubbled anhydrous hydrogen chloride gas until a solution resulted. After a solution resulted, the reaction was cooled in an ice bath and saturated with hydrogen chloride. The cooling bath was removed and the reaction stirred at room temperature for 3.5 hours. The solvent was removed on a rotary evaporator at ambient temperature and the resultant residue dissolved in methanol (25 ml), cooled in an ice bath and saturated with hydrogen chloride gas. Warming of the reaction solution to room temperature and removal of the solvent on a rotary evaporator gave an oil. To this oil was added triethylamine (15 ml) followed by the minimum amount of methanol (about 15 ml) needed to dissolve the initial gummy solid. The solution was cooled in an ice bath and ether (75 ml) added in portions with stirring. The precipitated triethylamine hydrochloride was filtered and the filtrate evaporated to give methyl (3S)-3-amino-2-hydroxybutanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05496927
Source datasetuspto-grants-1996_03
ORD IDord-c306b72d6756434a94dbf65ef447d9d3
Source noteuspto-grants-1996_03