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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641650Generated: November 1, 2026

Formaldehyde → (S)-5-biphenyl-4-ylmethyl-1-pyrrolidin-1-ylmethylpyrrolidin-2-one

https://huagongshe.com/reaction/1641650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantPyrrolidineHCID 31268—
Reactant(S)-5-[(biphenyl-4-yl)methyl]-1-(2,2-dimethylpropionyl)pyrrolidin-2-oneHCID 58160363—
SolventEthanolHCID 702—
Product(S)-5-biphenyl-4-ylmethyl-1-pyrrolidin-1-ylmethylpyrrolidin-2-oneHCID 59318460—

Reaction Steps

A mixture of 500 mg (S)-5-biphenyl-4-ylmethylpyrrolidin-2-one (1-a, R1=H), 329 μl pyrrolidine and 415 μl formaldehyde in 3.5 ml ethanol were heated at reflux for 3 h. A further quantity of 164 μl pyrrolidine and 148 μl formaldehyde were added and the mixture refluxed for about 24 h. The mixture was concentrated to dryness and purified by chromatography to obtain 533 mg of (S)-5-biphenyl-4-ylmethyl-1-pyrrolidin-1-ylmethylpyrrolidin-2-one (1-a, R1=methylpyrrolidin). 1H NMR (DMSO): 1.69 (4H, m, 2×NCH2CH2); 1.68-2.15 (4H, m, 3-CH2, 4-CH2); 2.50 (4H, 2×NCH2); 2.66 (1H, dd, 1-CHH); 3.12 (1H, dd, 1-CHH); 3.94 (1H, d, NCHHN); 4.21 (1H, d, NCHHN); 7.29 (2H, d, aromatic); 7.33 (1H, t, aromatic); 7.44 (2H, t, aromatic); 7.59 (2H, d, aromatic); 7.64 (2H, d, aromatic). m/z: 335 (MH+, 100%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08115016B2
Source datasetuspto-grants-2012_02
ORD IDord-f013c1651c62409b94aa3f8834f8cb63
Source noteuspto-grants-2012_02