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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1287362Generated: October 24, 2026

Sodium Sulfate → 3,5-Dimethyl-4-(hydroxymethyl)isoxazole

https://huagongshe.com/en/reaction/1287362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfateHCID 24436—
ReactantEthyl 3,5-dimethylisoxazole-4-carboxylateHCID 736348—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
Product3,5-Dimethyl-4-(hydroxymethyl)isoxazoleHCID 289575—

Reaction Steps

A suspension of 100 g (2.63 moles) of lithium aluminum hydride in 2.5 liters of anhydrous ether was stirred under nitrogen as a solution of 272 g. (1.61 mole) of the 4-carboethoxy-3,5-dimethylisoxazole prepared in Example 1 above in 400 ml. of anhydrous ether was added at such a rate as to maintain a gentle reflux. The suspension was stirred at room temperature under nitrogen overnight, during which time an extremely gummy green-gray mass formed in the bottom of the flask. The mixture was cooled in an ice bath and hydrolyzed with saturated aqueous sodium sulfate solution. Anhydrous sodium sulfate was added to dry the ether solution. The salts were removed by filtration and washed carefully with ether and chloroform. Solvent removal from the filtrates, finally at 50°/0.1 mm., gave a white crystalline mass. This was triturated with hot ether and then cooled. Filtration gave 3,5-dimethyl-4-hydroxymethyl-isoxazole as white prisms, m.p. 76.5°/77.5°. Concentration of the mother liquors gave a second crop of prisms, m.p. 76.5°-78°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03984428
Source datasetuspto-grants-1976_10
ORD IDord-ed38425886134226acc4429ca55b6429
Source noteuspto-grants-1976_10