Isocyanic acid → 3,6-Dibutyl-2,5-dimethylpyrazine
反応式
[N:1](=[C:3]([CH2:7][CH2:8][CH2:9][CH3:10])[C:4](=O)[CH3:5])O.[CH3:11][C:12](=O)[CH2:13][CH2:14][CH2:15][CH2:16][CH3:17].[N:19](Cl)=O.N=C=O>[Zn].C(O)(=O)C>[CH3:11][C:12]1[C:13]([CH2:14][CH2:15][CH2:16][CH3:17])=[N:19][C:4]([CH3:5])=[C:3]([CH2:7][CH2:8][CH2:9][CH3:10])[N:1]=1参加物
7
実験手順
e. 2,5-Dimethyl-3,6-dibutyl-pyrazine was prepared by first forming 3-oximino-2-heptanone by reacting 2-heptanone 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-dibutyl-pyrazine which had a b.p. of 18°C./0.002 mm. Hg.
出典と根拠
- ORDレコード
- ord-c273c6ffc3614cacb981034d91f88874
- 出典データセット
- uspto-grants-1976_03
- 特許番号
- US03943260
反応ノート
読み込み中…