HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium tert-butoxide → 2,2-dimethyl-2H-pyran-3,5(4H,6H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | Methyl 2-(1,1-dimethyl-2-oxopropoxy)acetate | HCID 85791200 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2,2-dimethyl-2H-pyran-3,5(4H,6H)-dione | HCID 14072887 | — |
Reaction Steps
A solution of potassium tert-butoxide (1M in tert-butanol, 12.1 mL, 12.1 mmol) in diethyl ether (7.5 mL) at 0° C. under N2 gas was treated with a solution of the product from Example 66B in diethyl ether (3 mL). After 10 minutes, the reaction mixture was quenched into 2N HCl (25 mL) and extracted with diethyl ether (3×25 mL). The organic layers were combined, washed with brine, dried over Na2SO4, concentrated to an oil, treated with 10% dichloromethane in hexane (5 mL), and placed in the freezer for 1 hour. The resulting crystals were collected by filtration, washed with a cold solution of 10% dichloromethane in hexane, and dried to provide the title compound (431 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06642222B2 |
| Source dataset | uspto-grants-2003_11 |
| ORD ID | ord-4c45c51cb5f74bb38ed1951dd5c0599e |
| Source note | uspto-grants-2003_11 |