HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 10469118, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3,5-Dimethyl-4-hydroxybenzonitrile | HCID 20176 | — |
| Reactant | HCID 19804385 | HCID 19804385 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 10469118 | HCID 10469118 | 66% |
Reaction Steps
To a mixture of 7.84 g 4-cyano-2,6-dimethylphenol, 3.57 g potassium hydroxide and 10.6 g potassium iodide in 200 ml acetonitrile was added 12 g 5-(2-chloropropyl)-3-ethylisoxazole, and the mixture was heated at reflux for about 16 hrs. The reaction mixture was concentrated in vacuo and the residue partitioned between ethyl acetate and water. The ethyl acetate layer was washed with aqueous sodium hydroxide (10%) until the excess starting phenol was removed, and the solution concentrated to give 10 g of 5-[3-(2,6-dimethyl-4-cyanophenoxy)propyl]-3-ethylisoxazole as a yellow oil. A sample of the latter was obtained in crystalline form, m.p. 50°-51° C. by crystallization from methanol at -50° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05175178 |
| Source dataset | uspto-grants-1992_12 |
| ORD ID | ord-4088dc8ed0e04f9690e4dd02d8893512 |
| Source note | uspto-grants-1992_12 |