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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898170Generated: October 30, 2026

Water → (S)-2,2-diphenyl-2-(pyrrolidin-3-yl)acetonitrile

https://huagongshe.com/reaction/898170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium formateHCID 2723923—
Reactant((S)-1-benzylpyrrolidin-3-yl)diphenylacetonitrile hydrochlorideHCID 66855790—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product(S)-2,2-diphenyl-2-(pyrrolidin-3-yl)acetonitrileHCID 2284283399.7%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of (S)-1-benzyl-3-(1-cyano-1,1-diphenylmethyl)pyrrolidine hydrochloride (8.55 g, 21.98 mmol) in methanol (44 mL) was added palladium on carbon (1.71 g) and ammonium formate (6.93 g, 109.9 mmol). The reaction mixture was heated to 50° C. with stirring for 3 h. The reaction was cooled to ambient temperature and water (20 mL) was added. The resulting mixture was filtered through a pad of Celite, washing with methanol (20 mL). The filtrate was collected and most of the methanol was removed in vacuo. The residue was mixed with isopropyl acetate (100 mL) and 10% aqueous sodium carbonate (50 mL). The resulting layers were separated and the aqueous layer was extracted with isopropyl acetate (50 mL). The organic layers were combined and dried over sodium sulfate (20 g). The sodium sulfate was filtered off and washed with isopropyl acetate (20 mL). The solvent was removed in vacuo to afford 5.75 g of the title intermediate as a light yellow oil (99.7% yield, 71% purity by HPLC).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07351717B2
Source datasetuspto-grants-2008_04
ORD IDord-bc2eaad70b4a46e794b247222dc036b6
Source noteuspto-grants-2008_04