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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604756Generated: October 26, 2026

Perillaldehyde → Perilla alcohol

https://huagongshe.com/reaction/1604756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPerillaldehydeHCID 16441—
ReactantSelenium DioxideHCID 24007—
Reactant(+)-LimoneneHCID 440917—
Catalystchromium (VI) trioxideHCID 10219390—
ProductPerilla alcoholHCID 369312—

Reaction Steps

Perillyl alcohol can be produced by reacting limonene with selenium dioxide (that is toxic) and other oxidants (that are difficult to work with i.e., anhydrous chromium trioxide) to yield various oxidation products, including a small amount of perillaldehyde. Once isolated, perillaldehyde is reduced to afford perillyl alcohol. While this two-step process is conceptually attractive, the oxidation of limonene to give perillyl alcohol proceeds in a low overall yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994598
Source datasetuspto-grants-1999_11
ORD IDord-efc8b7b2544149a1a9a6fdf90618994b
Source noteuspto-grants-1999_11