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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394907Generated: October 25, 2026

Pyridine → t-Butyl isobutyrylacetate

https://huagongshe.com/reaction/394907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
ReactantIsobutyryl chlorideHCID 62325—
SolventDichloromethaneHCID 6344—
Productt-Butyl isobutyrylacetateHCID 1097620557%

Reaction Conditions

Temperature0 °C

Reaction Steps

Meldrum's acid (80 g, 555 mmol) was dissolved in 600 mL of CH2Cl2 and cooled to 0° C. Freshly distilled pyridine (87.8 g, 1.11 mol) was added to the CH2Cl2 solution and then iso-butyryl chloride (65.0 g, 610.5 mmol) was added to the mixture via a pressure equalizing addition funnel. The reaction was stirred at 0° C. for 1 hr and then warmed to rt and stirred for 2 hr. Then, the reaction was quenched with water (200 mL) and washed with 0.5 M HCl (×2), water (×1), and brine (×1). The organize layer was dried over MgSO4 and concentrated in vacuo. The crude product was azeotropically dried with benzene (250 mL), and then dissolved in 200 mL of benzene and 200 mL of tert-butanol was added. The resultant reaction was heated at reflux for 4 hr. After this period, the volatiles were removed in vacuo and the product then distilled on the high vacuum pump (bp 62-63° C., 0.1 mm Hg). The desired β-keto ester 1E was obtained (58.6 g, 315.5 mmol) in 57% yield as a clear, colorless, light oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06603023B2
Source datasetuspto-grants-2003_08
ORD IDord-c2ab02a0095c4e6bbc13c7b7d5e2569b
Source noteuspto-grants-2003_08