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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824619Generated: October 26, 2026

4-Vinylbenzaldehyde → 4-Vinylbenzaldehyde

https://huagongshe.com/reaction/1824619

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-VinylbenzaldehydeHCID 39389—
ReactantHCID 178418634HCID 178418634—
SolventDimethylformamideHCID 6228—
Product4-VinylbenzaldehydeHCID 39389—
ProductBenzaldehyde, 2-ethenyl-HCID 39391—

Reaction Steps

Aldehyde 11 was synthesized by radical addition (Lub et al. (1997) Liebigs Ann. Recueil, 2281–2288) of thioacetic acid to 4-vinylbenzaldehyde. Vinyl benzaldehyde was synthesized by the procedure of Ren et al. (1993) Bull. Chem. Soc. Jpn. 66: 1897–1902 with the following changes: The addition of DMF was performed at a 38 mmol scale at 0° C. Purification by column chromatography (silica, Et2O/hexanes, 1:3) afforded 4-vinylbenzaldehyde in 60% yield (FIG. 37).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07042755B1
Source datasetuspto-grants-2006_05
ORD IDord-7634c165a21d451eaed7b282210961fa
Source noteuspto-grants-2006_05