Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 48105Generated: October 27, 2026

4-Pentylcyclohexanal → 2-Benzyloxy-6-[2-(4-pentyl-cyclohexyl)-vinyl]-naphthalene

https://huagongshe.com/reaction/48105

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PentylcyclohexanalHCID 14085659—
Reactant(6-Benzyloxynaphthalen-2-ylmethyl)-triphenyl-phosphonium BromideHCID 20632177—
ReactantPotassium tert-butoxideHCID 23665647—
Solventtert-Butyl methyl etherHCID 15413—
Product2-Benzyloxy-6-[2-(4-pentyl-cyclohexyl)-vinyl]-naphthaleneHCID 6988478874%

Reaction Steps

The solution of (6-benzyloxy-naphthalen-2-ylmethyl)-triphenyl-phosphonium bromide (19) (1 equi.), 4-pentyl-cyclohexanecarboxaldehyde (22), and potassium tert-butoxide (1.3 equi.) in tert-butyl methyl ether (6 mL/mmole) was stirred at room temperature for 24 h, then quenched with water, extracted with diethyl ether, washed with brine, dried over MgSO4, and concentrated in vacuo. Purification by chromatography on silica gel (1.25% EtOAc/hexane) afforded 2-benzyloxy-6-[2-(4-pentyl-cyclohexyl)-vinyl]-naphthalene (23) as a white solid (74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06703082B1
Source datasetuspto-grants-2004_03
ORD IDord-f6c63d21095849468799f3cf0417b9fa
Source noteuspto-grants-2004_03