HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-(1-Chloroethyl)-5-t-butylisoxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 1-(5-t-Butyl-isoxazol-3-yl)ethanol | HCID 57736312 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 3-(1-Chloroethyl)-5-t-butylisoxazole | HCID 57736302 | — |
Reaction Steps
1.18 g of 1-(5-t-butyl-isoxazol-3-yl)ethanol was dissolved in 2 ml of pyridine, and 1.36 of 4-toluenesulfonyl chloride was then added under ice-cooling. The mixture was stirred for 5 hours under ice-cooling. After water was added, the reaction mixture was extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate, filtered and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 1.60 g of 3-(1-chloroethyl)-5-t-butylisoxazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07846956B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-ac395ad5524a47ecbf37e8d382f3a00e |
| Source note | uspto-grants-2010_12 |