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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161612Generated: October 26, 2026

Geraniol → Citral

https://huagongshe.com/reaction/1161612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGeraniolHCID 637566—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
ProductCitralHCID 63801180%

Reaction Steps

Geraniol (7.0 g, 0.045 mol, 1 equiv.), manganese (IV) dioxide (100.0 g) and dichloromethane (500 ml) were stirred together at ambient temperature overnight. The mixture was filtered through Celite™, and the filtrate concentrated in vacuo to yield geranial (5.42 g, 80%). A cooled (−15° C.), stirred suspension of methyltriphenyl-phosphonium iodide (16.0 g, 0.039 mol, 1.1 equiv.) in tetrahydrofuran (50 ml) and diethyl ether (50 ml) was treated with n-butyllithium (2.5 M; 16 ml, 0.039 mol, 1.1 equiv.). After 0.25 hours, geranial (5.42 g, 0.036 mol, 1 equiv.) was added and the mixture allowed to stir at ambient temperature for 1 hour. The mixture was partitioned between diethyl ether (200 ml), water (200 ml) and petroleum ether b.p. 40-60° C. (200 ml), and the organic layer dried (MgSO4) and concentrated in vacuo to yield a crude oil which was subjected to column chromatography over Florisil (100% hexane) to give the nonatriene as a colourless oil (3.42 g, 64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820153B2
Source datasetuspto-grants-2010_10
ORD IDord-c97e769954354b0e9bbb3785df25d045
Source noteuspto-grants-2010_10