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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | (S)-5-[(biphenyl-4-yl)methyl]-1-(2,2-dimethylpropionyl)pyrrolidin-2-one | HCID 58160363 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (S)-5-biphenyl-4-ylmethyl-1-pyrrolidin-1-ylmethylpyrrolidin-2-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08115016B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-f013c1651c62409b94aa3f8834f8cb63 |
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| Source note | uspto-grants-2012_02 |
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