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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166811Generated: November 2, 2026

Pyridine → HCID 178442518, compound

https://huagongshe.com/reaction/2166811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantHCID 178442519HCID 178442519—
SolventDichloromethaneHCID 6344—
ProductHCID 178442518HCID 178442518—

Reaction Conditions

Temperature55 °C

Reaction Steps

6.0 Ml. of benzenesulfonyl chloride are added dropwise while stirring to a suspension of 10.8 g. of trans-4-[5-(p-n-heptylphenyl)-2-pyrimidinyl]cyclohexane carboxamide in 150 ml. of pyridine. The mixture is then warmed to 55° C. for 2 hours in an oil-bath. The mixture is poured into ice-water and the product is taken up in methylene chloride. The extract is washed successively with dilute hydrochloric acid, saturated sodium bicarbonate solution and water, dried over sodium sulfate and evaporated. The crude product is chromatographed on a column of 300 g. of silica gel with toluene/5% acetone (v/v). The fractions which are pure according to thin-layer chromatography are combined and evaporated. The residue is dissolved in hexane, filtered hot with active carbon and recrystallized. The crystallizate is dried in vacuo overnight. There is obtained trans-4-[5-(p-n-heptylphenyl)-2-pyrimidinyl]cyclohexane carbonitrile; melting point 83.5° C., clearing point 160° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04389329
Source datasetuspto-grants-1983_06
ORD IDord-01b8b15588b44536b9e1e9e51fd9a3bc
Source noteuspto-grants-1983_06