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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181083Generated: October 25, 2026

Acetic Acid → (2,2-Dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-acetic acid

https://huagongshe.com/reaction/2181083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant(Z)-2,2-Dimethyl-5-(tert-butyldiphenylsilyloxycarbonyl-methylene)-1,3-dioxolan-4-oneHCID 21947558—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(2,2-Dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-acetic acidHCID 6886064285.2%

Reaction Steps

A solution of pure (Z)-2,2 dimethyl-5-(t-butyldiphenylsilyloxycarbonylmethylene)-1,3-dioxolan-4-one (2.80 g, 6.82 mmol) in tetrahydrofuran (40 ml) was treated at 22° C. with acetic acid (2 ml) followed by 6.8 ml of a 1 M solution of tetrabutylammonium fluoride in tetrahydrofuran. After 15 minutes at 22° C., the reaction mixture was diluted with ethyl acetate, washed with water, brine and dried (magnesium sulfate). The solvent was concentrated under reduced pressure and the residue was triturated with toluene to give 1.00 g (85% yield) of the title compound as a white crystalline material: mp 203-204° C. (dec.). IR (KBr) v max (cm−1): 1805, 1707 and 1662. 1H NMR (400 MHz, CDCl3) δ: 1.78 (s, 6), 5.89 (s, 1). Anal. calcd for C7H805: C, 48.84; H, 4.68; Found: C, 48.84; H, 4.65.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06890942B2
Source datasetuspto-grants-2005_05
ORD IDord-2badf4da99284ed59575856d97fada77
Source noteuspto-grants-2005_05