HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 1-Benzyl-5-oxo-1,4,5,6-tetrahydro-cyclopentapyrazole-3-carboxylic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrazine, (phenylmethyl)-, hydrochloride (1:1) | HCID 14084 | — |
| Reactant | (4-Ethoxy-2-oxo-cyclopent-3-enyl)oxo-acetic acid tert-butyl ester | HCID 58713641 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Benzyl-5-oxo-1,4,5,6-tetrahydro-cyclopentapyrazole-3-carboxylic acid tert-butyl ester | HCID 58713645 | 62.1% |
Reaction Steps
To a solution of the intermediate from step A (2.15 g, 8.45 mmol) in ethanol (100 mL) was added benzyl hydrazine hydrochloride (1.8 g, 9.22 mmol) and HOAc (10 mL). The reaction mixture was stirred at room temperature for 16 hours and then refluxed at 70° C. for 30 minutes. The reaction was cooled to room temperature and concentrated in vacuo. The residue was dissolved in ethyl acetate and washed with water, saturated NaHCO3, and brine. The organic layer was dried over anhydrous Na2SO4 filtered and concentrated in vacuo. The residue was purified by flash chromatography (SiO2) using 30% ethyl acetate-hexanes to give the desired product (1.64 g) a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08637555B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-c726fce1cffe49cd853f5fc42cabe192 |
| Source note | uspto-grants-2014_01 |