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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286152Generated: October 30, 2026

Water → HCID 54359738, compound

https://huagongshe.com/reaction/2286152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-Methyl-2-butenalHCID 61020—
ReactantSodiumHCID 5360545—
ReactantHCID 12874246HCID 12874246—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54359738HCID 5435973856.1%

Reaction Steps

4.6 g (0.2 mol) of sodium were dissolved incrementally in 100 ml of dry ethanol. When all the sodium had dissolved, 100 ml of anhydrous tetrahydrofuran were added and 58.4 g (0.2 mol) of 4-methoxy-α-chloro-benzyl-phosphonic acid diethyl ester, dissolved in 50 ml of anhydrous tetrahydrofuran, were added dropwise at 0° C., while stirring. After stirring had been continued at 0°-10° C. for a further 1 hour, 16.8 g (0.2 mol) of β,β-dimethylacrolein, dissolved in 30 ml of anhydrous tetrahydrofuran, were added dropwise, while stirring. Stirring was then continued at room temperature for a further 12 hours. 600 ml of water were then added to the reaction mixture and the mixture was extracted twice with 300 ml of methylene chloride each time. The organic phase was separated off and dried over magnesium sulphate, the solvent was distilled off under a waterpump vacuum and the residue was distilled in vacuo. 25 g of 1-(4'-methoxyphenyl)-1-chloro-4,4-dimethyl-1,3-butadiene (isomer mixture) were obtained as a yellow oil which had a boiling point of 130°-145° C./2 mm Hg and partially crystallized after some time.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04327025
Source datasetuspto-grants-1982_04
ORD IDord-9c43ed414bcf4156909b3f8e7d9dcf8e
Source noteuspto-grants-1982_04