HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanethiol → HCID 15708214, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | HCID 22418871 | HCID 22418871 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 15708214 | HCID 15708214 | 85% |
Reaction Steps
597 mg of ethyl 2-(4-quinolylmethyl)acrylate was dissolved in 3 ml of ethylmercaptan. Then, 50 mg of potassium tert-butoxide was added thereto, and the mixture was stirred at room temperature for two hours. Then, the reaction solution was diluted with 60 ml of ethyl acetate and washed with 40 ml of water and then with 40 ml of a saturated sodium chloride aqueous solution. The organic layer was separated, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residual syrup was purified by silica gel column chromatography (n-hexane/ethyl acetate=5/2) and dried to obtain 640 mg (yield: 85%) of the desired product as syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05122523 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-99a63eb89de54d82b71404bc9661e4f0 |
| Source note | uspto-grants-1992_06 |