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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36149Generated: October 26, 2026

3-Bromophenol → Pentyl ether

https://huagongshe.com/reaction/36149

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromophenolHCID 11563—
ReactantPentyl etherHCID 12743—
ReactantBenzyl 5-Bromoamyl EtherHCID 14221121—
Reactant3-(Benzyloxypentyl)-phenolHCID 53906938—
ReactantHCID 178418306HCID 178418306—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductPentyl etherHCID 12743—
Product3-(5-Hydroxypentyl)-phenolHCID 22407972—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05412137
Source datasetuspto-grants-1995_05
ORD IDord-a33eb14b5e2546bc96b1dbc59ac08fd1
Source noteuspto-grants-1995_05