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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606233Generated: October 30, 2026

Pyridine → HCID 21388873, compound

https://huagongshe.com/reaction/1606233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantButyryl chlorideHCID 8855—
Reactant4'-Hydroxy-4-biphenylcarbonitrileHCID 140610—
SolventBenzeneHCID 241—
ProductHCID 21388873HCID 21388873—

Reaction Steps

0.390 G. of 4'-cyano-4-hydroxy-biphenyl are dissolved in 4.0 ml. of absolute pyridine and cooled to -10° with stirring. 0.255 G. of butyric acid chloride are added dropwise thereto over a period of 2 minutes. The temperature rises to 0° and pyridine hydrochloride precipitates out. Subsequently, the mixture is stirred overnight at room temperature and the suspension poured on to a mixture of 12 g. of ice and 12 ml. of 20% hydrochloric acid. Thereafter, this mixture is extracted three times with ethyl acetate, washed with water, dried over sodium sulfate and evaporated in vacuum. The 0.552 g. of yellowish crystals obtained as the residue are dissolved in benzene and chromatographed on 40 g. of silica gel. Benzene elutes 0.521 g. of yellowish crystals which are recrystallized from acetone-hexane up to constant melting point and clearing point. The pure 4'-cyano-4-biphenylyl butyrate obtained melts at 77.9°-78.2° and is liquid crystalline (monotrope) upon cooling to 74.7°. UV (EtOH): ε272 = 26,100.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03952046
Source datasetuspto-grants-1976_04
ORD IDord-f724e72e32e14ad5b59819017cfc5844
Source noteuspto-grants-1976_04