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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921928Generated: October 30, 2026

Ethyl Bromide → (Z)-2-(Ethoxymethylene)-4,4-dimethylpentanal

https://huagongshe.com/reaction/1921928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantMethyl formateHCID 7865—
ReactantSodium MethoxideHCID 10942334—
Reactant4,4-DimethylpentanalHCID 11062343—
SolventBenzeneHCID 241—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product(Z)-2-(Ethoxymethylene)-4,4-dimethylpentanalHCID 86627013—

Reaction Conditions

Temperature40 °C

Reaction Steps

4,4-Dimethylpentanal (4.20 g, 36.8 mmol, Step 2) in 36 mL of THF was added over 4 hours by syringe pump to a solution of sodium methoxide, 25 wt. % in methanol (15.1 ml, 66.2 mmol), 15 mL of methanol, and methyl formate (166 ml, 2685 mmol). Following the addition, the reaction was diluted with benzene (50 mL) and DMF (40 mL). The solvents were distilled off at 90° C. leaving the DMF and residual benzene. Bromoethane (11.0 ml, 147 mmol) was added and the solution was heated at 40° C. for 48 hrs and then cooled. The solution was diluted with water, and the reaction was extracted with ether. The combined organic layers were washed with water, brine, and dried over magnesium sulfate, filtered and concentrated toafford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173810B2
Source datasetuspto-grants-2012_05
ORD IDord-48ecdc6aa93a4796954773172a2c8933
Source noteuspto-grants-2012_05