HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896892Generated: October 26, 2026
Diethyl methylmalonate → 1-(3-bromophenyl)-5-hydroxy-4-methyl-1,2-dihydro-3H-pyrazol-3-one
https://huagongshe.com/reaction/896892
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl methylmalonate | HCID 11857 | — |
| Reactant | 3-Bromophenylhydrazine hydrochloride | HCID 33757 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(3-bromophenyl)-5-hydroxy-4-methyl-1,2-dihydro-3H-pyrazol-3-one | HCID 22351447 | 10.4% |
Reaction Steps
To a suspension of 1-(3-bromophenyl)hydrazine hydrochloride (1.0 g, 4.47 mmol) in ethanol (8.9 mL) was added dropwise 2.0 M sodium ethoxide in ethanol (0.77 mL, 9.84 mmol, 2.2 eq.). Diethyl 2-methylmalonate (0.85 mL, 4.92 mmol, 1.1 eq.) was then added. The reaction mixture was stirred at 90° C. for 16 hours and then quenched with 2 N aqueous hydrochloric acid (50 mL). The reaction was extracted with ethyl acetate (3×50 mL), and the combined organic layers were dried (MgSO4), filtered, and evaporated under reduced pressure. Purification using MPLC (Biotage) eluted with 3:1 v/v ethyl acetate-hexane gave the desired product as a white solid (125 mg, 0.46 mmol, 10.4% yield). MS LC-MS (ES MH+=269/271); TLC (Rf=0.10, 50% ethyl acetate-hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06919371B2 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-113b7167765c4b089b2ddabc67f843f6 |
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| Source note | uspto-grants-2005_07 |
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