HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870495Generated: October 27, 2026
L-Pyroglutamic Acid → (S)-5-Oxopyrrolidine-2-carboxamide
https://huagongshe.com/reaction/870495
Participants
| Role | Name | HCID | Charge |
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| Reactant | L-Pyroglutamic Acid | HCID 7405 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Hydroxybenzotriazole, ammonium salt | HCID 22033809 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (S)-5-Oxopyrrolidine-2-carboxamide | HCID 444439 | 98% |
Reaction Steps
To a stirred solution of L-pyroglutamic acid (II) (75 gm, 0.580 mol, commercially available) in dimethylformamide (750 ml) was added 1-hydroxy benzotriazole ammonium salt (106 gm, 0.696 mol, prepared according the literature procedure described in WO 2006100119) in one lot at 25° C. To this reaction mass, DCC was added in small portions over a period of 30 minutes at 0-5° C. The reaction mixture was allowed to warm to room temperature and stiffing continued further for 2 hours. The precipitates were removed by filtration and the filtrate concentrated under reduced pressure. The residue was treated with ethyl acetate (1000 ml) and stirred for 1 hour. The precipitate formed was filtered under suction and washed with additional ethyl acetate (2×75 ml). The combined filtrate was concentrated under reduced pressure to obtain 73 gm of (S)-5-oxopyrrolidine-2-carboxamide (III) as a white solid in 98% yield. The solid thus obtained was used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969567B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-f025474831a844149cf7665e111da56a |
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| Source note | uspto-grants-2015_03 |
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