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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416274Generated: October 30, 2026

Ethylene Glycol → Ethyl 5-(2-methyl-1,3-dioxolan-2-yl)isoxazole-3-carboxylate

https://huagongshe.com/reaction/416274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactant5-Acetyl-isoxazole-3-carboxylic acid ethyl esterHCID 2736353—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventBenzeneHCID 241—
ProductEthyl 5-(2-methyl-1,3-dioxolan-2-yl)isoxazole-3-carboxylateHCID 58930452100.1%

Reaction Steps

A reaction mixture consisting of ethyl 5-acetylisoxazole-3-carboxylate (2.53 g, 13.8 mmol), ethylene glycol (1.29 g, 20.7 mmol) and p-TsOH (0.13 g, 0.69 mmol) in benzene (50 mL) was refluxed with the Dean-Stark adapter for 24 hours (scheme 59). Most of the solvent was removed under reduced pressure and the residue was partitioned between saturated NaHCO3 and EtOAc. Organic layer was collected, washed with brine, water, and dried over MgSO4. Evaporation of the dried extract under reduced pressure afforded the title compound as an oil (3.14 g, 100% yield), which was used for next step without further purification. 1H NMR (DMSO-d6) δ (ppm): 6.89 (s, 1H), 4.35 (q, J=7.2 Hz, 2H), 4.07-4.01 (m, 2H), 4.01-3.94 (m, 2H), 1.70 (s, 3H), 1.32 (t, J=7.0 Hz, 3H). MS (m/z): 227.21 (calc) 228.1 (MH+) (found).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088805B2
Source datasetuspto-grants-2012_01
ORD IDord-f6bfd3162b91455da114214aad23ba38
Source noteuspto-grants-2012_01