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HRID 36149생성일: 2026년 10월 23일

3-Bromophenol → Pentyl ether

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

반응식

참여 물질

역할이름HCID투입량
반응물3-BromophenolHCID 11563—
반응물Pentyl etherHCID 12743—
반응물Benzyl 5-Bromoamyl EtherHCID 14221121—
반응물3-(Benzyloxypentyl)-phenolHCID 53906938—
반응물HCID 178418306HCID 178418306—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
용매TetrahydrofuranHCID 8028—
생성물Pentyl etherHCID 12743—
생성물3-(5-Hydroxypentyl)-phenolHCID 22407972—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05412137
출처 데이터셋uspto-grants-1995_05
ORD IDord-a33eb14b5e2546bc96b1dbc59ac08fd1
출처 메모uspto-grants-1995_05