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HRID 267653作成日:2026年10月24日

Isocyanic acid → 2,5-Dimethyl-3,6-dipropylpyrazine

https://huagongshe.com/ja/reaction/267653

反応式

関与物質

役割名称HCID仕込み量
反応物Isocyanic acidHCID 6347—
反応物2-HexanoneHCID 11583—
反応物Nitrosyl chlorideHCID 17601—
反応物3-Oximino-2-hexanoneHCID 71437750—
触媒ZincHCID 23994—
溶媒Acetic AcidHCID 176—
生成物2,5-Dimethyl-3,6-dipropylpyrazineHCID 596333—

反応手順

c. 2,5-Dimethyl-3,6-dipropyl-pyrazine was prepared by first forming 3-oximino-2-hexanone by reacting 2-hexanone with nitrosyl chloride according to the method of BOUVEAULT, Bull. [3] 31, 1163 (1904). The autocondensation of the two molecules of the imino-ketone in the presence of zinc and acetic acid [according to the method described in Chimia 11, 310 (1957)] yielded 2,5-dimethyl-3,6-dipropyl-pyrazine which had a b.p. of 109°-110°C./10 mm. Hg. (5) d. 2,5-Dimethyl-3,6-diisopropyl-pyrazine was prepared by first forming 4-methyl-3-oximino-2-pentanone by reacting 4-methyl-2-pentanone with nitrosyl chloride according to the method of BOUVEAULT, Bull. [3] 31, 1163 (1904). The autocondensation of two moles of the imino-ketone in the presence of zinc and acetic acid [according to the method described in Chimia 11, 310 (1957)] yielded 2,5-Dimethyl-3,6-diisopropyl-pyrazine which had a b.p. of 91°C./8 mm. Hg.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03943260
出典データセットuspto-grants-1976_03
ORD IDord-cbe2976501ac43218af39327464ba35d
出典メモuspto-grants-1976_03