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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478294Generated: October 25, 2026

Potassium tert-butoxide → 2,2-dimethyl-2H-pyran-3,5(4H,6H)-dione

https://huagongshe.com/reaction/478294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
ReactantMethyl 2-(1,1-dimethyl-2-oxopropoxy)acetateHCID 85791200—
SolventDiethyl EtherHCID 3283—
Product2,2-dimethyl-2H-pyran-3,5(4H,6H)-dioneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642222B2
Source datasetuspto-grants-2003_11
ORD IDord-4c45c51cb5f74bb38ed1951dd5c0599e
Source noteuspto-grants-2003_11