HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 19867638, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 86749404 | HCID 86749404 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 19867638 | HCID 19867638 | 65.2% |
Reaction Steps
A mixture of β-(4-fluorophenyl)-α-(2-methyl-1-oxopropyl)-δ-oxobenzenepentanoic acid, ethyl ester (7.92 gm, 20.6 mmol) and hydroxylamine hydrochloride (4.32 gm, 62.2 mmol) in glacial HOAc (100 ml) was refluxed for 2.5 hours. The reaction was cooled to room temperature and poured into an ice cold solution of concentrated NH4OH (140 ml) in H2O (400 ml). The resulting mixture was extracted twice with Et2O and the combined ethereal layers were washed with brine, dried (Na2 SO4), filtered and stripped to yield a gummy orange-red oil. Flash chromatography of the oil (Merck SiO2, 7% EtOAc in hexane) gave 4-(4-fluorophenyl)-2-(1-methylethyl)-6-phenyl-3-pyridinecarboxylic acid, ethyl ester (4.88 gm, 65%) as a near colorless gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05691322 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-87b642cf0091480993762342d4cb7a24 |
| Source note | uspto-grants-1997_11 |