HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 14456880, compound → HCID 53647417, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 14456880 | HCID 14456880 | — |
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 53647417 | HCID 53647417 | 21% |
Reaction Steps
A solution of 1-formyl-3-piperidinyl p-toluenesulfonate (1.12 g., 0.007 mole) and potassium thioacetate (0.91 g., 0.008 mole) in 10 ml. dimethylformamide was heated at 70° C. under nitrogen for 20 hours. The reaction mixture was diluted with 150 ml. ethyl acetate and the resulting solution was washed with four 50 ml. portions of water and 50 ml. brine, dried over anhydrous sodium acetate and concentrated in vacuo. The residue was chromatographed on silica gel (125 g.) eluting with 4:1 ethyl acetate-hexane to yield 0.16 g. (21% yield) of the title compound. NMR (CDCl3): 1.13-2.3 (c) and 2.32 (s) (total 7H); 2.84-4.0 (c, 5H); and 7.9 (d, 1H)ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04772597 |
| Source dataset | uspto-grants-1988_09 |
| ORD ID | ord-5fa8eb8e77514202ba2f3ca187f08960 |
| Source note | uspto-grants-1988_09 |