Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371351Generated: November 1, 2026

4-Hydroxybenzaldehyde → HCID 178444466, compound

https://huagongshe.com/reaction/2371351

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 178444473HCID 178444473—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178444466HCID 17844446660.3%

Reaction Steps

A mixture of 5.0 g of (E)-3-(trans-4-pentylcyclohexyl)allyl alcohol, 2.9 g of 4-hydroxybenzaldehyde, 4.1 g of diethyl azodicarboxylate, 6.2 g of triphenylphosphine and 100 ml of tetrahydrofuran was stirred at room temperature overnight and then concentrated. The residue was suspended in 300 ml of hexane, filtered and again concentrated. Chromatography of the residue on silica gel with toluene and recrystallization from hexane gave 4.5 g of pure 4-[(E)-3-(trans-4-pentylcyclohexyl)allyloxy]benzaldehyde with m.p. 55° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05093027
Source datasetuspto-grants-1992_03
ORD IDord-72124c6a43934d83b41b85ec7af9fde9
Source noteuspto-grants-1992_03