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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732729Generated: October 30, 2026

1,1-Dichloroethane → 4-({[(1R)-1-(3-methoxyphenyl)ethyl]amino}methyl)-1-phenylpyrrolidin-2-one hydrochloride

https://huagongshe.com/reaction/732729

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-DichloroethaneHCID 6365—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(R)-1-(3-Methoxyphenyl)ethylamineHCID 7020759—
Reactant5-Oxo-1-phenylpyrrolidine-3-carboaldehydeHCID 86628540—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product4-({[(1R)-1-(3-methoxyphenyl)ethyl]amino}methyl)-1-phenylpyrrolidin-2-one hydrochlorideHCID 68912462—

Reaction Steps

A 10 ml dichloroethane solution of 0.53 g of 5-oxo-1-phenylpyrrolidine-3-carboaldehyde was mixed with 508 mg of (1R)-1-(3-methoxyphenyl)ethanamine and 0.1 ml of acetic acid and stirred at room temperature for 1 hour. Successively this was mixed with 1.8 g of sodium triacetoxyborohydride and stirred overnight at room temperature. This was mixed with 40 ml of water and extracted with chloroform. The organic layer was concentrated, and the thus obtained residue was purified by a silica gel column chromatography (chloroform-methanol), treated with 4 M hydrogen chloride/ethyl acetate and concentrated to dryness to obtain 161 mg of 4-({[(1R)-1-(3-methoxyphenyl)ethyl]amino}methyl)-1-phenylpyrrolidin-2-one hydrochloride as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585886B2
Source datasetuspto-grants-2009_09
ORD IDord-41da784be8ca4e3f8064cc66b741faee
Source noteuspto-grants-2009_09