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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828651Generated: November 1, 2026

1-Acetoxy-2-bromoethane → HCID 17937804, compound

https://huagongshe.com/reaction/1828651

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Acetoxy-2-bromoethaneHCID 13564—
ReactantSodium hydrideHCID 24758—
Reactant3-Methoxybenzofuran-5-olHCID 17937806—
SolventDimethylformamideHCID 6228—
ProductHCID 17937804HCID 17937804—

Reaction Steps

164 mg (1.0 mmol) XXI and 48 mg (1.2 mmol, 60%) NaH were stirred for 30 mins. in 20 ml DMF at 0° C. 227 μl (2.0 mmol, 97%) 2-bromoethyl acetate were added to the resulting suspension which was then stirred for 72 h at room temperature. The reaction was quenched by addition of 3 ml saturated NH4Cl solution and the solvents were removed in vacuo. The residue was taken up in ethyl acetate and water, the aqueous phase was extracted twice with ethyl acetate and the combined organic phases were dried over Na2SO4. After column filtration (40 g SiO2, n-hexane:ethyl acetate=2:1, applied with ethyl acetate), XXII was obtained in a yield of 220 mg (0.88 mmol, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060109B2
Source datasetuspto-grants-2006_06
ORD IDord-fb0d77d99f1e4f6ba95eee8a48229bf9
Source noteuspto-grants-2006_06