HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491850Generated: October 29, 2026
Bromine → 3-(4-Bromo-pyrazol-1-yl)-4-methyl-benzoic acid ethyl ester
https://huagongshe.com/reaction/491850
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | 4-Methyl-3-pyrazol-1-yl-benzoic acid ethyl ester | HCID 58861336 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-(4-Bromo-pyrazol-1-yl)-4-methyl-benzoic acid ethyl ester | HCID 58861442 | 102.6% |
Reaction Steps
A solution of 3-hydrazino-4-methyl benzoic acid (1.0 g, 4.93 mmol), malonaldehyde(bismethylacetate) (0.82 mL, 4.93 mmol), and concentrated HCl (1 mL) in EtOH (20 mL) was heated to reflux for 4 h. After cooling to room temperature, the reaction was poured into ice water, neutralized with 2N NaOH, and extracted with CH2Cl2 (3×). The organic layers were dried over Na2SO4, filtered and concentrated to afford 4-methyl-3-pyrazol-1-yl-benzoic acid ethyl ester (536 mg, 47%) as a yellow oil. A solution of the pyrazole (536 mg, 2.33 mmol) and bromine (0.167 mL, 3.26 mmol) in CHCl3 (15 mL) was refluxed for 4.5 h then cooled to room temperature. The solvent was evaporated to an orange oil. Purification using chromatography on silica gel (1:1 EtOAc/hexanes) yielded 3-(4-bromo-pyrazol-1-yl)-4-methyl-benzoic acid ethyl ester (0.739 g, 99%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07531560B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-4b7d59e09c434d6bbef4f7c458658181 |
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| Source note | uspto-grants-2009_05 |
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