HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → Ethylthioethyl-2-chloro-5-(2-chloro-4-trifluoromethylphenoxy)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chloro-5-[2-chloro-4-(trifluoromethyl)phenoxy]benzoyl chloride | HCID 12799632 | — |
| Reactant | Ethylthioethanol | HCID 19024902 | — |
| Product | Ethylthioethyl-2-chloro-5-(2-chloro-4-trifluoromethylphenoxy)benzoate | HCID 12799646 | 53% |
Reaction Steps
In 20 ml tetrahydrofuran were dissolved 0.8 g (0.0075 mol) of ethyl thioethanol and 0.8 g (0.0079 mol) of triethylamine, and while heating to 60°-80° C., 1.6 g (0.0043 mol) of 2-chloro-5-(2-chloro-4-trifluoromethylphenoxy)benzoyl chloride was added. After 5-hour stirring, the resulting mixture was cooled, freed of the solvent under reduced pressure, and extracted with benzene. The extract was washed with a dilute aqueous solution of caustic soda and then with dilute hydrochloric acid, and dehydrated with sodiumsulfate. By concentration, 1.0 g (0.0023 mol) of the intended product was obtained as an oily substance; yield 53.0%, nD23 1.5500.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04334914 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-1050a243f08c4fdc88ebd265f0040270 |
| Source note | uspto-grants-1982_06 |