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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380464Generated: October 31, 2026

4-Phenylpiperidine → 1-Benzyl-3-(RS)-(4-phenylpiperidinylmethyl)-4-(RS)-(3-thienyl)pyrrolidine

https://huagongshe.com/reaction/380464

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PhenylpiperidineHCID 69873—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant1-Benzyl-3-(SR)-formyl-4-(RS)-(3-thienyl)pyrrolidineHCID 18364719—
Solvent1,1-DichloroethaneHCID 6365—
SolventTriethylamineHCID 8471—
Product1-Benzyl-3-(RS)-(4-phenylpiperidinylmethyl)-4-(RS)-(3-thienyl)pyrrolidineHCID 9953731115%

Reaction Steps

To a solution of 0.13 g (0.48 mmol) of 1-benzyl-3-(SR)-formyl-4-(RS)-(3-thienyl)pyrrolidine and 0.13 g (0.67 mmol) of 4-phenylpiperidine in 2 mL of dichloroethane and 0.1 mL of Et3N at rt was added 0.21 g (0.96 mmol) of sodium triacetoxyborohydride. After stirring for 3 h at rt, the reaction mixture was partitioned between CH2Cl2 and sat'd NaHCO3. The organic fraction was dried over Na2SO4, filtered and the filtrate was concentrated. The residue was purified by chomatography (silica, acetone: hexanes, 1:3) to give 0.23 g of the title compound. 1H NMR CDCl3) δ7.21-7.44 (m, 11H), 7.07-7.13 (m, 2H), 3.74 (d, 1H, J=12.8 Hz), 3.67 (d, 1H, J=13.1 Hz). Mass Spectrum (CI) m/e=417 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06303593B1
Source datasetuspto-grants-2001_10
ORD IDord-517a83f4c7a64873b438aa4ac63b579e
Source noteuspto-grants-2001_10