HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → N-methyl-5-phenacyl-3-phenyl-4isoxazole carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 3-phenyl-5-(beta-hydroxyphenethyl)-N-methyl-isoxazole-4-carboxamide | HCID 20305005 | — |
| Catalyst | chromium (VI) trioxide | HCID 10219390 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-methyl-5-phenacyl-3-phenyl-4isoxazole carboxamide | HCID 20304991 | — |
Reaction Steps
A suspension of 50 g. (0.155 mole) of 3-phenyl-5-(β-hydroxyphenethyl)-N-methyl-isoxazole-4-carboxamide and 800 ml. acetic acid at room temperature is treated dropwise rapidly with 18.4 g. (0.185 mole) of chromium trioxide in 185 ml. water. The resulting solution is stirred for 2 hours at room temperature and a portion of the acetic acid is removed in vacuo. The remainder is poured onto ice water and extracted with methylene chloride. The methylene chloride layer is washed with 2N sodium hydroxide, dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo. The solid residue is triturated with hot ether, cooled to 0° C. and filtered to give N-methyl-5-phenacyl-3-phenyl-4isoxazole carboxamide, m.p. 125° to 128° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04054653 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-f721dc96feed4855bf7fc7737e085a17 |
| Source note | uspto-grants-1977_10 |