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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351852Generated: October 31, 2026

Acetonitrile → 4-(Benzyloxy)-3-oxobutanenitrile

https://huagongshe.com/reaction/2351852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantEthyl 2-(benzyloxy)acetateHCID 290299—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
Product4-(Benzyloxy)-3-oxobutanenitrileHCID 14651911151.1%

Reaction Conditions

Temperature-78 °C

Reaction Steps

In a stream of argon, 156.2 ml (0.248 mole) of a solution of 1.6 moles of n-butyllithiumhexane was added to 150 ml of anhydrous tetrahydrofuran. The mixture was cooled to -78° C., and a solution of 15.8 ml (0.293 mole) of acetonitrile in 50 ml of anhydrous tetrahydrofuran was added dropwise. The mixture was stirred at -78° C. for 1 hour. A solution of 55.2 g (0.248 mole) of ethylbenzyloxyacetate in 100 ml of anhydrous tetrahydrofuran was added dropwise. The mixture was stirred at -78° C. for 15 minutes and at room temperature for 50 minutes. The mixture was then poured into 200 ml of ice water. The aqueous layer was washed with ether, acidified with concentrated hydrochloric acid, and extracted with ether. The ether layer was washed with water and a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give 70.9 g of crude 4-benzyloxy-3-ketobutanenitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04874760
Source datasetuspto-grants-1989_10
ORD IDord-ccf9c7b1ace64bb5a0e08062d3a41f33
Source noteuspto-grants-1989_10