HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanethiol → Methyl 2-chloro-3-ethylthiomethyl-4-methanesulfonylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 3-bromomethyl-2-chloro-4-methylsulfonylbenzoate | HCID 10969914 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Methyl 2-chloro-3-ethylthiomethyl-4-methanesulfonylbenzoate | HCID 15132839 | 98.6% |
Reaction Steps
To 100 ml of tetrahydrofuran, 1.3 g of ethanethiol and 1.5 g of potassium carbonate and then 4.4 g of methyl 3-bromomethyl-2-chloro-4-methanesulfonylbenzoate were added, and the mixture was stirred for 1 day at room temperature. Then, the mixture was stirred further for 1 hour at a temperature of from 50° to 60° C. After cooling, chloroform was added thereto, and the mixture was washed with a dilute potassium carbonate aqueous solution. The chloroform layer was separated and dried. Then, the solvent was distilled off to obtain 4.1 g of methyl 2-chloro-3-ethylthiomethyl-4-methanesulfonylbenzoate as an oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04885022 |
| Source dataset | uspto-grants-1989_12 |
| ORD ID | ord-dfd71aef5be84e7288d737f2d2554e31 |
| Source note | uspto-grants-1989_12 |