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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743997Generated: November 4, 2026

Ethyl bromoacetate → HCID 19421373, compound

https://huagongshe.com/reaction/743997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
ReactantHCID 19421374HCID 19421374—
SolventDimethylformamideHCID 6228—
ProductHCID 19421373HCID 1942137393,750.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05559105
Source datasetuspto-grants-1996_09
ORD IDord-966d6ca0eaa743c5ad3ef7dc92506758
Source noteuspto-grants-1996_09