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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2089662Generated: October 26, 2026

Dichloromethane → 2,2-Dimethylmalonic acid t-butyl ester (2,2-dimethylpropyl)ester

https://huagongshe.com/reaction/2089662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantNeopentyl alcoholHCID 6404—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant3-(Tert-butoxy)-2,2-dimethyl-3-oxopropanoic acidHCID 254415—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
Solventtert-Butyl methyl etherHCID 15413—
Product2,2-Dimethylmalonic acid t-butyl ester (2,2-dimethylpropyl)esterHCID 86677399—

Reaction Steps

To a mixture of 2,2-dimethylmalonic acid mono-t-butyl ester (10 g), 2,2-dimethyl-1-propanol [CAS No. 75-84-3] (5.15 g), DMAP (1.3 g), and dichloromethane (100 mL), WSC (12.2 g) was added with stirring under ice-cooling, and the resulting mixture was stirred at room temperature for 2 days. TBME and water were added to the mixture, and the resulting mixture was extracted. The organic layer was sequentially washed with water and saturated aqueous sodium chloride solution, and dried over anhydrous magnesium sulfate. The desiccant was filtered off, and the filtrate obtained was concentrated under reduced pressure. The residue obtained was purified by silica gel column chromatography (mixed solvent of heptane-ethyl acetate) to obtain 2,2-dimethylmalonic acid t-butyl ester(2,2-dimethylpropyl)ester (12 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436009B2
Source datasetuspto-grants-2013_05
ORD IDord-9c026640a7af4bcfa1c86a1ce392f220
Source noteuspto-grants-2013_05