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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 1,3,5-Trioxane | HCID 8081 | — |
| Reactant | HCID 66643629 | HCID 66643629 | — |
| Reactant | HCID 178418365 | HCID 178418365 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Isobutoxy-5-methyl-isoxazole-4-carboxylic acid | HCID 66643699 | 32.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08357703B2 |
|---|
| Source dataset | uspto-grants-2013_01 |
|---|
| ORD ID | ord-645bcfc8a51546dab68eb819d2704c22 |
|---|
| Source note | uspto-grants-2013_01 |
|---|