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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290776Generated: October 30, 2026

HCID 13690971, compound → HCID 13690972, compound

https://huagongshe.com/reaction/2290776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 13690971HCID 13690971—
ReactantPotassium ethanethioateHCID 23670855—
SolventDimethylformamideHCID 6228—
ProductHCID 13690972HCID 1369097295.9%

Reaction Steps

To a solution of 2.44 g of 3-(2-chloroethyl)-5-(3-fluoro-4-phenyl-α-methylbenzyl)-1,2,4-oxadiazole in 40 ml of DMF was added 1.69 g of potassium thioacetate. After stirring at room temperature overnight, the reaction mixture was poured into ice-water. The resultant mixture was extracted with benzene and the organic phase was washed with water, dried over sodium sulfate and evaporated under reduced pressure. The residue was chromatographed over silica gel using benzene to yield 2.62 g of 3-(2-acetylthioethyl)-5-(3-fluoro-4-phenyl-α-methylbenzyl)-1,2,4-oxadiazole as a light brown oil. It was crystallized from diisopropyl ether to give colorless needles, m.p. 56°-57° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04618617
Source datasetuspto-grants-1986_10
ORD IDord-980effae0380436ea97e2a0965f67dbd
Source noteuspto-grants-1986_10