HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 4-Acetoxy-3-pyridine-4-yl-4-m-tolyl-cyclopent-2-en-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 4-Hydroxy-3-pyridine-4-yl-4-m-tolyl-cyclopent-2-en-1-one | HCID 21266447 | — |
| Reactant | 4-Hydroxy-4-pyridine-4-yl-3-m-tolyl-cyclopent-2-en-1-one | HCID 21266548 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Acetoxy-3-pyridine-4-yl-4-m-tolyl-cyclopent-2-en-1-one | HCID 21266556 | — |
Reaction Steps
To a solution of 4-hydroxy-4-pyridine-4-yl-3-m-tolyl-cyclopent-2-en-1-one, and it's regioisomer 4-hydroxy-3-pyridine-4-y1-4-m-toly1-cyclopent-2-en-1-one prepared as described in Example 8, Step E (265 mg, 1.0 mmole) in methylene chloride (5 mL) was added dimethylamino pyridine (183 mg, 1.5 mmole) and acetic anhydride (0.12 mL, 1.2 mmole) at r.t. The reaction mixture was stirred at that temperature for 1 hr before quenching the reaction with 1 mL of methanol. Concentration and purification (silica, hexane/ethyl acetate) gave the title compound as the slower eluting isomer. MS (m/z): Calcd. C19H17NO3(M+): 307, found (M+H) +: 308.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06174901B1 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-8ad9a94d686d46bdb219eae6e7d60c80 |
| Source note | uspto-grants-2001_01 |