HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 2-[p-(phenylthio)phenoxy]ethylthiocarbamic acid S-ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl chlorothioformate | HCID 18056 | — |
| Reactant | 2-[p-(Phenylthio)phenoxy]ethylamine | HCID 23350121 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-[p-(phenylthio)phenoxy]ethylthiocarbamic acid S-ethyl ester | HCID 54204522 | 76% |
Reaction Steps
7 g of 2-[p-(phenylthio)phenoxy]ethylamine and 18.6 g of chlorothioformic acid S-ethyl ester are dissolved in 250 ml of acetone. 24 g of potassium carbonate are added to the solution and the mixture is heated under reflux for 6 hours. The mixture is then filtered, the residue is washed with acetone and the filtrate is evaporated in vacuo. The 13 g of residue are filtered through a 10-fold amount of silica gel with ether/cyclohexane (7:3). The first fractions yielded 10.2 g which, after recrystallization from ether/low boiling petroleum ether yields 6.3 g (76%) of 2-[p-(phenylthio)phenoxy]ethylthiocarbamic acid S-ethyl ester, m.p.--77°-79° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04215139 |
| Source dataset | uspto-grants-1980_07 |
| ORD ID | ord-0d9bfb391cb74699bfd4162923edab52 |
| Source note | uspto-grants-1980_07 |