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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27994Generated: October 30, 2026

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

https://huagongshe.com/reaction/27994

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 ethanl, which had been prepared from 1.5 g of sodium and 30 ml of ethanol, while stirring at room temperature. After dropping the resultant 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 numberUS04224450
Source datasetuspto-grants-1980_09
ORD IDord-9c98732d38e645a6be69603cd1e65629
Source noteuspto-grants-1980_09