Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1977706Generated: October 31, 2026

Phenyl cyanate → 4-(p-Chlorophenyl)-4-methyl-2-pentynenitrile

https://huagongshe.com/reaction/1977706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl cyanateHCID 70740—
ReactantHCID 15431059HCID 15431059—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
SolventSodium HydroxideHCID 14798—
Product4-(p-Chlorophenyl)-4-methyl-2-pentynenitrileHCID 2199553481.3%

Reaction Conditions

Temperature10 °C

Reaction Steps

A solution of 1,1-dibromo-3-(p-chlorophenyl)-3-methyl-1-butene (38.5 g, 0.113 mol) in tetrahydrofuran is treated with n-butyllithium (0.25 mol, 100 mL of a 2.5 M solution in hexane) under nitrogen over 45 minutes while maintaining the temperature below −65° C., stirred overnight at dry ice/acetone bath temperature, treated dropwise with a solution of phenyl cyanate (14.89 g, 0.125 mol) in tetrahydrofuran over 30 minutes at −65° C. to −70° C., allowed to warm to 10° C., and diluted with ethyl acetate and 5% sodium hydroxide solution. The resultant mixture is extracted with ethyl acetate. The organic extracts are combined, washed sequentially with 5% sodium hydroxide solution and water, dried over anhydrous sodium sulfate and concentrated in vacuo to obtain a residue. The residue is distilled to give the title product as an oil (18.7 g, bp 110-113° C./0.9 mm Hg, 80.7% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06235754B1
Source datasetuspto-grants-2001_05
ORD IDord-c37c751d289f4dbd9cffab2a148ce3cc
Source noteuspto-grants-2001_05