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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392815Generated: October 27, 2026

Acetic Acid → Z-2,2-dimethyl-5-carboxymethylene-1,3-dioxolan-4-one

https://huagongshe.com/reaction/392815

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—
ProductZ-2,2-dimethyl-5-carboxymethylene-1,3-dioxolan-4-oneHCID 1163688885.2%

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%) 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 C7H8O5: C, 48.84; H, 4.68. found: C, 48.84; H, 4.65.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06803378B2
Source datasetuspto-grants-2004_10
ORD IDord-f9795dc884644b4797b29dba8d60b1d3
Source noteuspto-grants-2004_10