HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526688Generated: October 27, 2026
Propanoic acid, 2-bromo-2-methyl-, ethyl ester → HCID 89907301, compound
https://huagongshe.com/reaction/526688
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propanoic acid, 2-bromo-2-methyl-, ethyl ester | HCID 11745 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | [5-(2,4-Dichloro-phenyl)-2-methyl-6-(4-trifluoromethyl-phenyl)-pyridin-3-yl]-methanol | HCID 89907741 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 89907301 | HCID 89907301 | — |
Reaction Steps
To a solution of 500 mg of [5-(2,4-Dichloro-phenyl)-2-methyl-6-(4-trifluoromethyl-phenyl)-pyridin-3-yl]-methanol in 6 ml of DMF were added 242 mg of sodium hydride (60% in mineral oil) at room temperature. After 15 min, 448 mg of tetrabutylammonium iodide and 946 mg 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: 200 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09346757B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-5faf061e990b4b6fbe876e69eebfe214 |
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| Source note | uspto-grants-2016_05 |
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