HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 31551Generated: October 25, 2026
Ethyl Acetate → Ethyl 2-[2-(4-bromophenyl)ethoxy]-2-methylpropionate
https://huagongshe.com/reaction/31551
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Propanoic acid, 2-bromo-2-methyl-, ethyl ester | HCID 11745 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(4-Bromophenyl)ethanol | HCID 72851 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 2-[2-(4-bromophenyl)ethoxy]-2-methylpropionate | HCID 59792867 | 15.2% |
Reaction Steps
To a solution of 2-(4-bromophenyl)ethanol (1 g, 5 mmol) in THF (15 ml) was added sodium hydride (60% in parafin liquid) (220 mg, 5.5 mmol) at 0° C., and the mixture was stirred at room temperature for 15 minutes. To the mixture was added ethyl 2-bromoisobutyrate (1.08 g, 5.5 mmol), and the mixture was stirred at room temperature for 12 hours. To this reaction solution were added ethyl acetate and a saturated aqueous ammonium chloride solution, and the organic layer was separated. The aqueous layer was extracted twice with ethyl acetate, and the extracts were combined with the organic layer. The organic layer was collected, dried over anhydrous sodium sulfate, filtered, and the solvent was evaporated under reduced pressure. The resultant was purified by silica gel column chromatography (hexane:ethyl acetate=10:1) to give the title compound (240 mg, 15%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07425642B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-f165681782f44475b0ce8dcc89e8ab70 |
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| Source note | uspto-grants-2008_09 |
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