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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702693Generated: October 26, 2026

1-Bromohexadecane → 4-Hexadecylaminobenzoylacetonitrile

https://huagongshe.com/reaction/1702693

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromohexadecaneHCID 8213—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzenepropanenitrile, 4-amino-beta-oxo-HCID 96920—
SolventHexamethylphosphoramideHCID 12679—
Product4-HexadecylaminobenzoylacetonitrileHCID 20525834—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of p-aminobenzoylacetonitrile, 1-bromohexadecane, potassium carbonate and hexamethylphosphoramide is heated to 80° C. for 20 hours and worked up as in Example 1, providing 4-hexadecylaminobenzoylacetonitrile. This material is dissolved in isopropanol and treated with an excess of sodium borohydride. After stirring at room temperature for 3 hours, the solution is concentrated, diluted with water and extracted with chloroform. The chloroform extract yields the crude carbinol which is heated to reflux for 1 hour with ethanol containing an equal volume of 2 N aqueous hydrochloric acid. The solution is then cooled, diluted with water and extracted with chloroform. The organic extract is washed successively with water and aqueous sodium bicarbonate, then dried and evaporated to afford 4-(hexadecylamino)cinnamonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04348399
Source datasetuspto-grants-1982_09
ORD IDord-6c0f44f169134eb7bf22eae09570c292
Source noteuspto-grants-1982_09