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HRID 487862作成日:2026年10月27日

3-Methyl-1-pentanol → Pyridine, 3-(4-methylhexyl)

https://huagongshe.com/reaction/487862

反応式

関与物質

役割名称HCID仕込み量
反応物3-Methyl-1-pentanolHCID 11508—
反応物3-HexylpyridineHCID 22766—
反応物Phosphorus tribromideHCID 24614—
反応物1-Bromo-3-methylpentaneHCID 39899—
溶媒PyridineHCID 1049—
溶媒Diethyl EtherHCID 3283—
生成物Pyridine, 3-(4-methylhexyl)HCID 529404—

反応手順

3-(4-Methylhexyl)pyridine was prepared in a similar manner to that described above with regard to 3-hexylpyridine but using 3-methyl-1-pentylbromide [prepared by adding over 1 h, at -30° C. and under N2, 22.5 g of PBr3 (0.083 mol; 7.8 ml) to a mixture of 21.6 g (0.212 mol) of 3-methyl-1-pentanol, 3.95 g of anhydrous pyridine and 88.4 ml of anhydrous sulfuric ether; the mixture was allowed to react for 1 h at -30° C. and then for 1 night at room temperature; the reaction product was extracted and washed in the usual manner and purified on a Vigreux column to provide 20.8 g of pure product].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05298486
出典データセットuspto-grants-1994_03
ORD IDord-1734eb148fa443828db0fb93bfafbdac
出典メモuspto-grants-1994_03