HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500440Generated: November 2, 2026
Triethylamine → (S)-5-biphenyl-4-ylmethyl-1-pyrrolidin-1-ylmethylpyrrolidin-2-one
https://huagongshe.com/reaction/1500440
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (S)-4-Amino-5-biphenyl-4-yl-pentanoic acid ethyl ester hydrochloride | HCID 66738936 | — |
| Solvent | Isopropyl Acetate | HCID 7915 | — |
| Product | (S)-5-biphenyl-4-ylmethyl-1-pyrrolidin-1-ylmethylpyrrolidin-2-one | HCID 59318460 | — |
Reaction Steps
To a mixture of (S)-4-Amino-5-biphenyl-4-yl-pentanoic acid ethyl ester hydrochloride[10-a, R5=Et] (86 g) in isopropyl acetate (1 L) is added triethylamine (43 g). The mixture is then stirred at about 55° C. for 1 h and then filtered. The filtrate is heated at reflux for 24 hours. To the mixture is added saturated ammonium chloride solution and the phases are separated. The organic layer is concentrated to dryness and crystallized from isopropyl acetate to yield (S)-5-biphenyl-4-ylmethylpyrrolidin-2-one [Key Lactam (1-a, R1=H)]. Spectroscopic data agree with data provided above.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09206116B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-bc25073e31834ba9af7825c50aa90df1 |
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| Source note | uspto-grants-2015_12 |
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