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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396849Generated: October 26, 2026

Benzyl chloroformate → 1-Benzyl 3-tert-butyl 1,3-pyrazolidinedicarboxylate

https://huagongshe.com/reaction/1396849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactanttert-butyl 4,5-dihydro-1H-pyrazole-5-carboxylateHCID 86706338—
SolventAcetic AcidHCID 176—
Product1-Benzyl 3-tert-butyl 1,3-pyrazolidinedicarboxylateHCID 1334154062.2%

Reaction Steps

To a solution of 1,1-dimethylethyl 4,5-dihydro-1H-pyrazole-5-carboxylate (5 g, 29.4 mmol) dissolved in acetic acid (75 mL) was added sodium cyanoborohydride (3.69 g, 58.8 mmol) over 10 minutes. After 30 min. the reaction mixture was concentrated. The intermediate was diluted with ethyl acetate and basified with sat. Na2CO3. The ethyl acetate was dried over sodium sulfate, filtered, and concentrated. The intermediate was diluted with tetrahydrofuran (THF) (75 mL), and triethylamine was added (8.19 mL, 58.8 mmol), followed by Cbz-Cl (2.1 mL, 14.69 mmol). After 2 h, the organic salts were filtered and the crude product was purified by silica gel column using 20-80% EtOAc/hexanes to afford 2.8 g (9.14 mmol) of 3-(1,1-dimethylethyl) 1-(phenylmethyl) 1,3-pyrazolidinedicarboxylate. LC-MS (ES) m/e 307.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901119B2
Source datasetuspto-grants-2014_12
ORD IDord-4c5479cb6874406b8589312dda7b85f6
Source noteuspto-grants-2014_12