HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384375Generated: October 29, 2026
Hydrochloric Acid → 2-(3-Ethyl-indan-5-yl)-5-methyl-2,4-dihydro-pyrazol-3-one
https://huagongshe.com/reaction/384375
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | di-tert-butyl 1-(3-ethyl-2,3-dihydro-1H-inden-5-yl)hydrazine-1,2-dicarboxylate | HCID 57483834 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | 2-(3-Ethyl-indan-5-yl)-5-methyl-2,4-dihydro-pyrazol-3-one | HCID 57483783 | 39.8% |
Reaction Steps
Di-tert-butyl 1-(3-ethyl-2,3-dihydro-1H-inden-5-yl)hydrazine-1,2-dicarboxylate 41c (3.43 g, 9.1 mmol) was dissolved in 50 mL of a solvent mixture of ethanol/water (V:V=3:2) followed by addition of 3-oxo-butanoic acid ethyl ester (1.18 g, 9.1 mmol) and 4.55 mL of hydrochloric acid (6 N). Upon completion of the addition, the reaction mixture was heated to reflux and reacted for 1 hour. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was concentrated under reduced pressure to remove ethanol and then extracted with dichloromethane (15 mL×3). The combined organic extracts were dried over anhydrous sodium sulfate, filtered to remove the drying agent and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to obtain the title compound 2-(3-ethyl-indan-5-yl)-5-methyl-2,4-dihydro-pyrazol-3-one 41d (0.712 g, 39.8%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367710B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-19e8ae138afe409aabf4c3d50b772909 |
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| Source note | uspto-grants-2013_02 |
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