HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (3,4-Dichloroisothiazol-5-yl)methyl benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (3,4-Dichloroisothiazol-5-yl)methanol | HCID 16723166 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (3,4-Dichloroisothiazol-5-yl)methyl benzoate | HCID 23658604 | 87.3% |
Reaction Steps
3.0 g (16.3 mmol) of the above-produced (3,4-dichloroisothiazol-5-yl)methanol and 2.52 g (17.9 mmol) of benzoyl chloride were dissolved in 70 ml of toluene. Thereto was dropwise added, under ice-cooling, 1.98 g (19.6 mmol) of triethylamine. The mixture was stirred at room temperature for 3 hours. Water was added, followed by extraction with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate, and concentrated. The resulting crystals were washed with hexane to obtain 4.1 g (yield: 87%) of (3,4-dichloroisothiazol-5-yl)methyl benzoate as colorless crystals (melting point: 79 to 80° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08003675B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-eabea0dbe4404a639aeb9a1e478a5cde |
| Source note | uspto-grants-2011_08 |