HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 22221447, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 22221006 | HCID 22221006 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22221447 | HCID 22221447 | 53% |
Reaction Steps
To a solution of 5-(2,5-dichlorophenyl)-4-isoxazolylmethanol (3.80 g) in toluene (60 ml) was added dropwise thionyl chloride (2.78 g) at 0° C. and the mixture was stirred at room temperature for 2 hr. The reaction mixture was concentrated, saturated aqueous sodium hydrogencarbonate was added to the residue, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography, and 4-chloromethyl-5-(2,5-dichlorophenyl)isoxazole (2.15 g, yield 53%) was obtained as an oil from a fraction eluted with ethyl acetate-hexane (1:9, volume ratio). NMR (CDCl3) δ: 4.45 (2H, s), 7.4–7.55 (3H, m), 8.48 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07022725B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-46fde503cdc446d9aa62df1daf6854d7 |
| Source note | uspto-grants-2006_04 |