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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728297Generated: November 2, 2026

Water → 3-Amino-3-[1-(4-chlorophenyl)cyclobutyl]propan-1-ol

https://huagongshe.com/reaction/728297

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 3-amino-3-[1-(4-chlorophenyl)cyclobutyl]propanoateHCID 19823680—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
Product3-Amino-3-[1-(4-chlorophenyl)cyclobutyl]propan-1-olHCID 19823871—

Reaction Steps

A solution of ethyl 3-amino-3-[1-(4-chlorophenyl)cyclobutyl]propanoate (5 g prepared as described in Example 137) in ether (25 ml) was added dropwise to a stirred suspension of lithium aluminium hydride (3 g) in ether (50 ml). The mixture was heated under reflux for 3 hours, allowed to stand for 16 hours with no heating and then heated under reflux for a further 6 hours. Water (3 ml) was added dropwise with stirring to the cooled reaction mixture followed by 15% aqueous sodium hydroxide solution (3 ml) and water (9 ml). The reaction mixture was filtered and the residue washed with ether. The filtrate and the washings were combined, washed with water then brine and dried. Evaporation of the solvent gave a residue which was recrystallised from petroleum ether (b.p. 40°-60° C.) to give 3-amino-3-[1-(4-chlorophenyl)cyclobutyl]propan-1-ol (m.p. 98°-99° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05047432
Source datasetuspto-grants-1991_09
ORD IDord-064b250ca91549e1a6adf0f2fce315ea
Source noteuspto-grants-1991_09