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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | tert-butyl 4,5-dihydro-1H-pyrazole-5-carboxylate | HCID 86706338 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-Benzyl 3-tert-butyl 1,3-pyrazolidinedicarboxylate | HCID 13341540 | 62.2% |
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
| 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-4c5479cb6874406b8589312dda7b85f6 |
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| Source note | uspto-grants-2014_12 |
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