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HRID 128377作成日:2026年10月26日

Diethyl Oxalate → 2-Oxohexanoic Acid

https://huagongshe.com/reaction/128377

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl OxalateHCID 7268—
反応物Ethyl hexanoateHCID 31265—
生成物2-Oxohexanoic AcidHCID 159664—

反応手順

Ethyl n-hexanoate and diethyl oxalate were subjected to Claisen condensation, and then hydrolyzed to form 2-oxo-n-hexanoic acid. This product was then condensed with diaminomaleonitrile to form 9.1 g (0.042 mole) of 2,3-dicyano-5-hydroxy-6-n-pentylpyrazine (m.p. 61°-64° C.). The product was dissolved in 120 g of phosphorus oxychloride, and 3.32 g (0.042 mole) of pyridine was added. The mixture was refluxed for 5 hours, and then worked up in the same way as in Example 3 and the resulting oily product was concentrated under reduced pressure. The resulting product was chromatographed on a silica gel column with benzene as an eluent to afford 6.0 g (yield 61%) of 2,3-dicyano-5-chloro-6-n-pentyl-pyrazine as a yellow liquid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04259489
出典データセットuspto-grants-1981_03
ORD IDord-1cd0839dd27f4a348367a4e7dd8b5e04
出典メモuspto-grants-1981_03