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HRID 1030028作成日:2026年10月27日

p-Bromophenyl octyl ether → 2-[4-(Octyloxy)-phenyl]-5-[(tetrahydro-2-pyranyloxy)methyl]pyridine

https://huagongshe.com/reaction/1030028

反応式

関与物質

役割名称HCID仕込み量
反応物p-Bromophenyl octyl etherHCID 145298—
反応物Sodium BicarbonateHCID 516892—
反応物MagnesiumHCID 5462224—
反応物2-Chloro-5-{[(oxan-2-yl)oxy]methyl}pyridineHCID 22127378—
触媒Diphenylphosphane;diphenyl(propan-2-yl)phosphane;nickel;chlorideHCID 21654969—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物2-[4-(Octyloxy)-phenyl]-5-[(tetrahydro-2-pyranyloxy)methyl]pyridineHCID 1982124567.2%

反応手順

A Grignard reagent solution prepared from 0.8 g of magnesium, 10.3 g of (4-bromophenyl) octyl ether and 50 ml of tetrahydrofuran was added dropwise at 0°-5° C. within 30 minutes to a mixture of 7.5 g of crude 2-chloro-5-[(tetrahydro-2-pyranyloxy)methyl]pyridine, 75 ml of tetrahydrofuran and 0.36 g of 1,3-bis(diphenylphosphino)-propanenickel-(II) chloride. The reaction mixture was stirred for 3 hours, left to stand overnight, then adjusted to pH 8 with aqueous sodium hydrogen carbonate solution and diluted with diethyl ether. The organic phase was washed neutral with water, dried over sodium sulfate and concentrated. Chromatographic purification of the residue (14.6 g) on 210 g of silica gel with hexane/ethyl acetate (vol. 4:1) yielded 8.8 g of 2-[4-(octyloxy)-phenyl]-5-[(tetrahydro-2-pyranyloxy)methyl]pyridine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05104569
出典データセットuspto-grants-1992_04
ORD IDord-353edb4686bd4b7699d7958b0d957b13
出典メモuspto-grants-1992_04