HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743997Generated: November 4, 2026
Ethyl bromoacetate → HCID 19421373, compound
https://huagongshe.com/reaction/743997
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 19421374 | HCID 19421374 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19421373 | HCID 19421373 | 93,750.5% |
Reaction Steps
To a mixture of NaH (80% oil dispersion, 33 mg, 1.1 mmol, previously washed with hexanes), in DMF (4 ml) was added dropwise a solution of 2-n-butyl-5-(2-Hydroxy-4-methoxybenzoyl)-1-trimethylsilylethyloxymethoxy-1H-imidazole-(404 mg, 1.00 mmol) in DMF (3 ml) at 0° under argon. The cooling bath was removed and the mixture stirred for 10 min. at ambient temperature. Ethyl bromoacetate (125 μl, 1.10 mmol) was added neat and the reaction stirred for 2 h. The mixture was partitioned between water and EtOAc and the layers separated. The aqueous layer was further extracted (EtOAc, 2x) and the combined organic extract was washed with water (5x) and brine. Evaporation under reduced pressure, after drying (MgO4 anhydrous) afforded the title compound as a reddish oil (475 g, 97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05559105 |
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| Source dataset | uspto-grants-1996_09 |
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| ORD ID | ord-966d6ca0eaa743c5ad3ef7dc92506758 |
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| Source note | uspto-grants-1996_09 |
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