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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881882Generated: October 27, 2026

Citric Acid → 2-[2-(1,3-Dioxolan-2-yl)-1,3-thiazol-5-yl]-1,1-dimethoxypropan-2-ol

https://huagongshe.com/reaction/1881882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantPyruvic aldehyde dimethyl acetalHCID 80650—
Reactant2-(1,3-Dioxolan-2-yl)-1,3-thiazoleHCID 15205158—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
Product2-[2-(1,3-Dioxolan-2-yl)-1,3-thiazol-5-yl]-1,1-dimethoxypropan-2-olHCID 5933161390.2%

Reaction Conditions

Temperature-70 °C

Reaction Steps

To a solution of 2-(1,3-dioxolan-2-yl)-1,3-thiazole (1.00 g) in tetrahydrofuran (20 mL) was slowly added a 1.6M n-butyllithium hexane solution (4.5 mL) at −70° C. under a nitrogen atmosphere. The reaction mixture was stirred at −70° C. for 30 min, and 1,1-dimethoxypropan-2-one (1.50 g) was added. The reaction mixture was warmed to room temperature, 10% aqueous citric acid solution was added, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The obtained residue was subjected to silica gel column chromatography, and the title compound (1.58 g, yield 90%) was obtained as a yellow oil from a fraction eluted with ethyl acetate-hexane (9:1, volume ratio). MS: 276 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318746B2
Source datasetuspto-grants-2012_11
ORD IDord-508054894adc44b097df154dab71a0ef
Source noteuspto-grants-2012_11