HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → Ethyl 2-(4-t-Butylphenylthio)octanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Tert-Butylbenzenethiol | HCID 75454 | — |
| Reactant | Ethyl 2-bromooctanoate | HCID 95580 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl 2-(4-t-Butylphenylthio)octanoate | HCID 14995385 | 57% |
Reaction Steps
A mixture of 5.0 g (0.02 mole) ethyl 2-bromooctanoate, 3.37 g (0.02 mole) p-t-butylthiophenol and 3.31 g (0.24 mole) potassium carbonate in 70 ml acetone was refluxed under nitrogen overnight. The reaction mixture was cooled to room temperature and filtered and the filtrate was concentrated in vacuo. The residue was chromatographed on 500 g silica gel, eluting with 6:4 methylene chloride/hexane to yield 3.8 g (57% yield) of the desired product as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05656634 |
| Source dataset | uspto-grants-1997_08 |
| ORD ID | ord-2b03c1ed92614a51bfc64c6129588c3d |
| Source note | uspto-grants-1997_08 |