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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749599Generated: October 30, 2026

Hydrochloric Acid → HCID 11687105, compound

https://huagongshe.com/reaction/749599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-[1-(4-chlorophenyl)ethylidene]malononitrileHCID 263676—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
ProductHCID 11687105HCID 1168710556.1%

Reaction Steps

First, 3.00 g of (4-chloro-α-methylbenzylidene)malononitrile was dissolved in 20 ml of ethanol, and while stirring at room temperature, a suspension of 0.15 g of sodium borohydride in 5 ml of ethanol was added dropwise, followed by stirring at room temperature for 30 minutes. Then, 10% hydrochloride acid was added to the reaction mixture, which was extracted with diethyl ether. The organic layer was successively washed with 10% hydrochloric acid, a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 1.70 g of (1-(4-chlorophenyl)ethyl)malononitrile (the intermediate (6)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07402691B2
Source datasetuspto-grants-2008_07
ORD IDord-8c8ee4e1f9054cd1951d118cea2b07b7
Source noteuspto-grants-2008_07