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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzyl succinimido carbonateHCID 83172—
Reactanttert-Butyl pyrazolidine-3-carboxylateHCID 57015512—
SolventDichloromethaneHCID 6344—
Product1-Benzyl 3-tert-butyl 1,3-pyrazolidinedicarboxylateHCID 13341540110.9%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901119B2
Source datasetuspto-grants-2014_12
ORD IDord-dd9ee9b5f3b3499ab6e2c46b0b678b09
Source noteuspto-grants-2014_12