HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396846Generated: October 26, 2026
Triethylamine → 1-Benzyl 3-tert-butyl 1,3-pyrazolidinedicarboxylate
https://huagongshe.com/reaction/1396846
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzyl succinimido carbonate | HCID 83172 | — |
| Reactant | tert-Butyl pyrazolidine-3-carboxylate | HCID 57015512 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Benzyl 3-tert-butyl 1,3-pyrazolidinedicarboxylate | HCID 13341540 | 110.9% |
Reaction Steps
At 0° C., to a 50 mL round bottomed flask charged with 1,1-dimethylethyl 3-pyrazolidinecarboxylate (0.054 g, 0.259 mmol) and stirrer in dichloromethane (DCM) (3 mL), was added triethylamine (0.079 mL, 0.569 mmol). After a couple of minutes, N-(benzyloxycarbonyloxy)succinimide (CBz-OSu) (0.064 g, 0.259 mmol) in dichloromethane (DCM) (1.5 mL) was added dropwise. The reaction mixture stirred at 0° C. for one hour, then warmed to r.t. After 2 hr at r.t., the solvent was evaporated and the residue was dissolved in EtOAc (30 mL), washed with water (15 mL×2), sat. NaHCO3 (15 ml), brine (15 mL), dried over Na2SO4 and concentrated to afford the crude product as a colorless gum (88 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08901119B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-dd9ee9b5f3b3499ab6e2c46b0b678b09 |
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| Source note | uspto-grants-2014_12 |
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