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HRID 36149作成日:2026年10月24日

3-Bromophenol → Pentyl ether

https://huagongshe.com/ja/reaction/36149

反応式

関与物質

役割名称HCID仕込み量
反応物3-BromophenolHCID 11563—
反応物Pentyl etherHCID 12743—
反応物Benzyl 5-Bromoamyl EtherHCID 14221121—
反応物3-(Benzyloxypentyl)-phenolHCID 53906938—
反応物HCID 178418306HCID 178418306—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
溶媒TetrahydrofuranHCID 8028—
生成物Pentyl etherHCID 12743—
生成物3-(5-Hydroxypentyl)-phenolHCID 22407972—

反応手順

At a temperature of -78° C., 19.4 ml of t-butyl lithium (1.7M) is added to 4.0 gm of the above 3-bromo-phenol, n-pentyl ether in 50 mls tetrahydrofuran; and to this is added 3.3 ml of a freshly prepared solution of Li2CuCl3 (0.10M/THF). The mixture is stirred for 10 minutes, and then 4.35 grams of the 1-bromo-5-benzyloxy pentane are added. The reaction is allowed to warm slowly to ambient temperature over 12 hours and is then stirred an additional 24 hours before being quenched with silica gel. After removing the solvent, the mixture is chromatographed over silica gel (1:1 hexane:ether) to yield a crude mixture containing 3-(benzyloxypentyl)-phenol, n-pentyl ether. A solution of 6.0 gm of this crude mixture in ethanol is hydrogenated over 5% Pd on carbon for 5 hours. After filtering through celite and concentrating, pure 3-(5-hydroxypentyl)-phenol, n-pentyl ether is obtained as a clear oil by HPLC chromatography.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05412137
出典データセットuspto-grants-1995_05
ORD IDord-a33eb14b5e2546bc96b1dbc59ac08fd1
出典メモuspto-grants-1995_05