HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1962333Generated: October 30, 2026
Sodium hydride → Methyl 2-(2-acetyl-5-bromophenoxy)acetate
https://huagongshe.com/reaction/1962333
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | 1-(4-Bromo-2-hydroxyphenyl)ethan-1-one | HCID 10727403 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 2-(2-acetyl-5-bromophenoxy)acetate | HCID 57419482 | 82% |
Reaction Steps
A solution of 1-(4-bromo-2-hydroxyphenyl)ethanone (1.35 g, 6.28 mmol) in anhydrous DMF (16 mL) was treated in several portions with sodium hydride (377 mg of 60% in oil, 226 mg, 9.42 mmol) followed by stirring at room temperature for 30 min. The mixture was then treated with methyl bromo-acetate (871 μL, 1.45 g, 9.48 mmol) dropwise (solution became warm after addition was complete) followed by stirring at room temperature for 18 h. The mixture was diluted with ethyl acetate and extracted with water (4×) and saturated sodium chloride solution. Drying (Na2SO4) and concentration in vacuo afforded a nearly colorless solid, which was purified by column chromatography on silica gel, eluting with 20-100% ethyl acetate in hexanes. These procedures afforded the title compound as a colorless solid (1.47 g, 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08415351B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-1b75ea6f982a4941ac4c18c2ba088a94 |
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| Source note | uspto-grants-2013_04 |
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