HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297073Generated: October 30, 2026
Water → (S)-2,2-diphenyl-2-(pyrrolidin-3-yl)acetonitrile
https://huagongshe.com/reaction/1297073
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | ((S)-1-benzylpyrrolidin-3-yl)diphenylacetonitrile hydrochloride | HCID 66855790 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (S)-2,2-diphenyl-2-(pyrrolidin-3-yl)acetonitrile | HCID 22842833 | 99.7% |
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 MeOH (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 hours. 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 MeOH (20 mL). The filtrate was collected and most of the MeOH was removed in vacuo. The residue was mixed with IPAc (100 mL) and 10% aqueous sodium carbonate (50 mL). The resulting layers were separated and the aqueous layer was extracted with IPAc (50 mL). The organic layers were combined and dried over sodium sulfate (20 g). The sodium sulfate was filtered off and washed with IPAc (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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07250414B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-d8640de5445f4035b9be0b13df0a16fa |
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| Source note | uspto-grants-2007_07 |
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