HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526703Generated: October 27, 2026
Propanoic acid, 2-bromo-2-methyl-, ethyl ester → HCID 89907577, compound
https://huagongshe.com/reaction/526703
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propanoic acid, 2-bromo-2-methyl-, ethyl ester | HCID 11745 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | [1-(2,4-Dichloro-phenyl)-4-methyl-5-(4-trifluoromethyl-phenyl)-1H-pyrazol-3-yl]-methanol | HCID 89907507 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 89907577 | HCID 89907577 | — |
Reaction Steps
To a solution of 2 g of [1-(2,4-Dichloro-phenyl)-4-methyl-5-(4-trifluoromethyl-phenyl)-1H-pyrazol-3-yl]-methanol in 15 ml of DMF were added 997 mg of sodium hydride (60% in mineral oil) at room temperature. After 15 min 1.8 g of tetrabutylammonium iodide and 2.9 g of 2-Bromo-2-methyl-propionic acid ethyl ester were added and the reaction mixture was stirred for 16 h at room temperature. After dilution with saturated aqueous sodium hydrogen carbonate solution the reaction mixture was filtered through a chem Elut® cartridge by eluting with ethyl acetate. The solvents were removed under reduced pressure and the crude product was purified by chromatography on silica gel eluting with a gradient of n-heptane/ethyl acetate. The fractions containing the product were combined and the solvent evaporated under reduced pressure. Yield: 1.3 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09346762B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-e03e763485fe4deaa5af0708476c9b2a |
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| Source note | uspto-grants-2016_05 |
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