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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290775Generated: October 31, 2026

Pyridine → HCID 13690971, compound

https://huagongshe.com/reaction/2290775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 20230259HCID 20230259—
SolventBenzeneHCID 241—
ProductHCID 13690971HCID 1369097187.9%

Reaction Steps

To a solution of 2.62 g of 5-(3-fluoro-4-phenyl-α-methylbenzyl)-3-(2-hydroxyethyl)-1,2,4-oxadiazole in 60 ml of dry benzene was successively added 2.0 g of thionyl chloride and 0.67 g of pyridine with ice-cooling. After stirring and heating with reflux for 1 hour, the reaction mixture was washed with water. The organic phase was further washed with water, dried over sodium sulfate and evaporated. The residue was chromatographed over silica gel using benzene to give 2.44 g of 3-(2-chloroethyl)-5-(3-fluoro-4-phenyl-α-methylbenzyl)-1,2,4-oxadiazole, m.p. 72°-72.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04618617
Source datasetuspto-grants-1986_10
ORD IDord-efe5f6e3ab4143a381b0bf9432138082
Source noteuspto-grants-1986_10