HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 3-(2-bromoethoxy)-2-methylbenzoate → Ethyl 3-(2-methylsulfonylthioethoxy)-2-methylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 3-(2-bromoethoxy)-2-methylbenzoate | HCID 15376195 | — |
| Reactant | Potassium thiomethanesulfonate | HCID 23696406 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 3-(2-methylsulfonylthioethoxy)-2-methylbenzoate | HCID 15376196 | — |
Reaction Steps
2 g (7 mmol) of ethyl 3-(2-bromoethoxy)-2-methylbenzoate and 1.1 g (7.3 mmol) of potassium thiomethanesulfonate are dissolved in 10 ml absolute ethanol. The reaction mixture is refluxed for 20 hours. The solvent is then distilled off and the residue taken up in methylene chloride and washed with water. The organic phase is dried over sodium sulfate and the solvent is removed. The product of value is purified by column chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05925767 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-971a12ba684246ea9e0f633a678e70d6 |
| Source note | uspto-grants-1999_07 |