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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2219219Generated: October 30, 2026

Ethyl Acetate → HCID 58816128, compound

https://huagongshe.com/reaction/2219219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant4-Bromobenzyl alcoholHCID 70119—
ReactantEthane, 2-bromo-1,1-diethoxy-HCID 74852—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 58816128HCID 5881612856%

Reaction Steps

Sodium bis(trimethylsilyl)amide (12.1 mL, 1 N in THF) is added to a stirred solution of 4-bromo-benzylalcohol (2.05 g, 11.0 mmol) in dry DMF (7 mL) at ambient temperature. The mixture is stirred for 5 min before it is treated with bromoacetaldehyde diethyl acetal (1.99 mL, 13.2 mmol). The resultant mixture is allowed to stir at ambient temperature for 20 hours. Ethyl acetate (60 mL) and water (60 mL) are added to the mixture. The organic layer is separated, washed with half-saturated brine, dried, filtered and concentrated. After MPLC separation on silica (gradient 0-8% ethyl acetate in hexane), 1.86 g (56% yield) title compound is obtained as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07414063B2
Source datasetuspto-grants-2008_08
ORD IDord-1922388f7efc4bb48d2dbcbf25a9cdef
Source noteuspto-grants-2008_08