HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553682Generated: October 30, 2026
Methyl iodide → Ethyl 2-(4-bromophenyl)propanoate
https://huagongshe.com/reaction/553682
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | Ethyl 2-(4-bromophenyl)acetate | HCID 7020609 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 2-(4-bromophenyl)propanoate | HCID 13840376 | — |
Reaction Steps
To ethyl 4-bromophenylacetate (2.137 g, 8.8 mmol) in THF (20 mL) at −78° C. was added lithium bis(trimethylsilyl)amide (1M in hexane; 11.4 mL, 11.4 mmol), and the solution was stirred for 1 hour at −78° C. Iodomethane (0.71 mL, 11.4 mmol) in THF (5 mL) was added, and the reaction was warmed to room temperature. The mixture was quenched with water and concentrated. The residue was dissolved in EtOAc and washed three times with water and once with brine. The organic layer was dried and concentrated, and the crude material was purified by silica gel chromatography (0-60% EtOAc in hexanes) to give 2-(4-bromo-phenyl)-propionic acid ethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08048902B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-c0b7bf1678a842dab93e77500fab5897 |
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| Source note | uspto-grants-2011_11 |
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