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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35791Generated: October 30, 2026

4-Hydroxybenzaldehyde → HCID 178444466, compound

https://huagongshe.com/reaction/35791

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 numberUS05411676
Source datasetuspto-grants-1995_05
ORD IDord-809683dd41704cbfb29138b53a6357df
Source noteuspto-grants-1995_05