HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 13690971, compound → HCID 13690972, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 13690971 | HCID 13690971 | — |
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13690972 | HCID 13690972 | 95.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04618617 |
| Source dataset | uspto-grants-1986_10 |
| ORD ID | ord-980effae0380436ea97e2a0965f67dbd |
| Source note | uspto-grants-1986_10 |