Methyl iodide → 4-[(Ethylthio)methyl]-1-methyl-1,2,3,6-tetrahydropyridine
反応式
[CH2:1]([S:3][CH2:4][C:5]1[CH:10]=[CH:9][N:8]=[CH:7][CH:6]=1)[CH3:2].[CH3:11]I>C(#N)C>[CH2:1]([S:3][CH2:4][C:5]1[CH2:6][CH2:7][N:8]([CH3:11])[CH2:9][CH:10]=1)[CH3:2]参加物
4
実験手順
8.2 g (0.054 mol) of 4-[(ethylthio)methyl]pyridine are dissolved in 60 ml of acetonitrile and then 9.1 g of methyliodide are added. After 12 hours the reaction mixture is evaporated down in vacuo. The residue is reacted analogously to Example 1 b) with sodium borohydride in methanol and worked up. The crude product obtained is distilled (5.2 g; 56.3% of theory; b.p. 118°-120° C./20 mbar) and then chromatographed on neutral aluminium oxide using chloroform as eluant. 4.4 g of 4-[(ethylthio)methyl]-1-methyl-1,2,3,6-tetrahydropyridine are obtained, which is converted with one equivalent of maleic acid into the maleate (m.p. 102°-105° C., from ethyl acetate).
後処理
- customAfter 12 hours the reaction mixture is evaporated down in vacuo
- customThe residue is reacted analogously to Example 1 b) with sodium borohydride in methanol
- customThe crude product obtained
- distillationis distilled (5.2 g; 56.3% of theory; b.p. 118°-120° C./20 mbar)
- customchromatographed on neutral aluminium oxide
出典と根拠
- ORDレコード
- ord-833ce92ccfa44f91b77719638dad4bee
- 出典データセット
- uspto-grants-1995_06
- 特許番号
- US05422353
反応ノート
読み込み中…