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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807535Generated: November 1, 2026

Carbon Dioxide → 3-Isobutoxy-5-methyl-isoxazole-4-carboxylic acid

https://huagongshe.com/reaction/1807535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant1,3,5-TrioxaneHCID 8081—
ReactantHCID 66643629HCID 66643629—
ReactantHCID 178418365HCID 178418365—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-Isobutoxy-5-methyl-isoxazole-4-carboxylic acidHCID 6664369932.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 4-iodo-3-isobutoxy-5-methyl-isoxazole (669 mg, 2.38) in THF (10 mL) at −30° C. and under argon was added isopropylmagnesium bromide (1.49 mL of a 2.0 M solution in THF) dropwise. The reaction mixture was warmed to 0° C. and stirred for 1 h, then 1,3,5-trioxane (429 mg, 4.76 mmol) in THF (1 mL) was added and the reaction mixture warmed to 50° C. After 1.5 h to the reaction mixture was added further 1,3,5-trioxane (860 mg, 9.52 mmol) and the reaction mixture heated at 70° C. After 2 h the mixture was cooled to 0° C. and solid CO2 (˜10 g) added. After 1 h the reaction mixture was diluted with water (15 mL) then extracted with diethylether. The aqueous phase was acidified with HCl (1 N, 10 mL), then the resultant precipitate filtered off and washed with water (5 mL), then dried under vacuum (60° C.) to afford the title compound (152 mg, 32%) as a white solid. MS: m/e=198.4 [M−H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357703B2
Source datasetuspto-grants-2013_01
ORD IDord-645bcfc8a51546dab68eb819d2704c22
Source noteuspto-grants-2013_01