HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-(4-Chlorophenyl)-2,1-benzisoxazole-7-acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 3-(4-Chlorophenyl)-7-(bromomethyl)-2,1-benzisoxazole | HCID 15634756 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(4-Chlorophenyl)-2,1-benzisoxazole-7-acetonitrile | HCID 15634758 | 61% |
Reaction Steps
A solution of 11.5 g (0.036 mole) of crude 3-(4-chlorophenyl)-7-(bromomethyl)-2,1-benzisoxazole, 9.8 g (0.15 mole) of potassium cyanide, 150 ml of dioxane and 75 ml of water was heated at reflux under a nitrogen atmosphere for 2.5 hr. The solution was cooled and poured into 400 ml of methylene chloride. The layers were separated and the organic layer was washed with four 200 ml portions of water, dried over sodium sulfate, and concentrated to give a solid as residue. The solid was recrystallized (charcoal) twice from ethyl acetate to yield 5.8 g (61%) of crystals, m.p. 165°-169° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04898874 |
| Source dataset | uspto-grants-1990_02 |
| ORD ID | ord-aaa339ad2e124f8c975149d421083d32 |
| Source note | uspto-grants-1990_02 |