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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2428142Generated: October 30, 2026

2,2-Dimethyl-1,3-dioxane-4,6-dione → HCID 67148305, compound

https://huagongshe.com/reaction/2428142

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
ReactantTriethylammonium formateHCID 11084032—
Reactant3-(tert-Butyl-dimethyl-silanyloxymethyl)-4-chloro-benzaldehydeHCID 137329917—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 67148305HCID 6714830587%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 3-(tert-butyl-dimethyl-silanyloxymethyl)-4-chloro-benzaldehyde (1.84 g, 6.46 mmol), Meldrum acid (931 mg, 6.46 mmol), and formic acid-triethylamine 5:2 complex (1.62 mL, 23.4 mmol) in DMF (6.00 mL) was heated to 100° C. for 3.5 h. Meldrum acid (466 mg, 3.23 mmol) was added again, and the mixture was stirred for 1 h at 100° C. The mixture was allowed to cool to rt, and was diluted with a mixture of water and ice. The resulting mixture was extracted several times with EtOAc. The combined org. extracts were washed with water, dried over MgSO4, filtered, and the solvents were removed under reduced pressure. The residue was dissolved in Et2O, and the resulting mixture was extracted several times with aq. 1M NaOH. The combined aq. extracts were acidified to pH 2 with aq. 1M HCl, and this aq. mixture was extracted back with Et2O several times. The combined org. extracts were dried over MgSO4, filtered, and the solvents were removed under reduced pressure. Drying the residue under high vacuum yielded the crude title compound (1.20 g, 87%) that was used further without purification. LC-MS: tR=0.71 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968720B2
Source datasetuspto-grants-2011_06
ORD IDord-b8daed818c664f0ea29932971ab0b2cd
Source noteuspto-grants-2011_06