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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725600Generated: November 1, 2026

Ethanol → HCID 14200631, compound

https://huagongshe.com/reaction/1725600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantDiethyl MalonateHCID 7761—
Reactanto-Bis(bromomethyl)benzeneHCID 66665—
ReactantSodium MethoxideHCID 10942334—
CatalystSulfuric AcidHCID 1118—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
ProductHCID 14200631HCID 1420063154.2%

Reaction Conditions

Temperature200 °C

Reaction Steps

A solution of α,α′-dibromo-o-xylene (203.51 g, 0.77 mol) in 1.5 l of ether is added to a solution of diethyl malonate (127 g, 0.79 mol), sodium methoxide (314 ml, 1.70 mol), ethanol (100 ml) and ether (500 ml). The mixture is refluxed for 5 hours, then filtered, and finally concentrated. The residue is taken up in 500 ml of water. 173 g of potassium hydroxide are added, and the mixture is refluxed for 18 hours. The reaction medium is poured into a hydrochloric acid solution and the precipitate formed is filtered off by suction and then dried. The solid obtained is maintained at 200° C. for 20 minutes and the new solid obtained is recrystallised from 400 ml of heptane. The crystals obtained are taken up in 400 ml of methanol and, after 5 drops of concentrated sulfuric acid have been added, the mixture is refluxed for 4 hours and then concentrated. The residue is dissolved in 600 ml of ether. This ether phase is washed with saturated sodium bicarbonate solution and saturated sodium chloride solution and then dried over sodium sulfate and concentrated, giving 73.6 g (54%) of a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491733B2
Source datasetuspto-grants-2009_02
ORD IDord-7676cad80a7f4b298cc437ff3f615030
Source noteuspto-grants-2009_02