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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389259Generated: October 30, 2026

Nitromethane → (3-Methylisoxazole-5-yl)glyoxal-2-oxim

https://huagongshe.com/reaction/1389259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitromethaneHCID 6375—
ReactantSodium ethoxideHCID 2723922—
ReactantSodiumHCID 5360545—
Reactant3-Methyl-1,2-oxazole-5-carbaldehydeHCID 10582758—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
Product(3-Methylisoxazole-5-yl)glyoxal-2-oximHCID 8876196870.8%

Reaction Steps

In 50 ml of ethanol were dissolved 5.5 g of 3-methylisoxazole-5-carbaldehyde and 3.3 g of nitromethane. To the solution was added dropwise a solution of sodium ethoxide in ethanol, which had been prepared from 1.5 g of sodium and 30 ml of ethanol, while stirring at room temperature. After completion of the dropwise addition, the resultant solution was stirred for a further 3 hrs. at room temperature and then ether was added thereto to separate the sodium salt. This was dissolved in water, which was followed by acidification with hydrochloric acid. The resulting precipitate was filtered off and recrystallized from chloroform to obtain 5.4 g of (3-methylisoxazole-5-yl)glyoxal-2-oxim having m.p. of 179° C.-180° C. Yield, 70%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04243812
Source datasetuspto-grants-1981_01
ORD IDord-7bf5ffd5eb9c46a6b06846330667a66f
Source noteuspto-grants-1981_01