HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668419Generated: November 1, 2026
Phenethylamine → (S)-2-Oxo-5-phenethylcarbamoyl-pyrrolidine-1-carboxylic acid benzyl ester
https://huagongshe.com/reaction/1668419
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenethylamine | HCID 1001 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-(Phenylmethyl) (2S)-5-oxo-1,2-pyrrolidinedicarboxylate | HCID 637648 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-2-Oxo-5-phenethylcarbamoyl-pyrrolidine-1-carboxylic acid benzyl ester | HCID 57612752 | — |
Reaction Steps
(S)-5-Oxo-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester (14.9 g, 57 mmol) is suspended in dichloromethane (100 mL) and added DMAP (7.1 g, 58 mmol) while cooling on ice (0-5° C.). The suspension immediately clarified. EDCI (11.1 g, 58 mmol) is added resulting in precipitation which quickly clarified again. Phenethylamine (6.8 mL, 54 mmol) is added slowly via syringe. The reaction is complete in one half hour. The dichloromethane layer is washed with aqueous 10% citric acid, water and saturated bicarb, then dried over anhydrous sodium sulfate, filtered and concentrated to a white solid. LCMS characterization ES+367.1 (m+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989441B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-4f1e8a73cb34449180ba72306e66a5ab |
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| Source note | uspto-grants-2011_08 |
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