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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5665Generated: October 26, 2026

Water → 2-(1-Methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenenitrile

https://huagongshe.com/reaction/5665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactanta FarnesolHCID 3327—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantPhosphonic acid, (1-cyano-2-methylpropyl)-, diethyl esterHCID 11031342—
SolventTolueneHCID 1140—
Product2-(1-Methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenenitrileHCID 5365714596%

Reaction Conditions

Temperature-70 °C

Reaction Steps

To a solution of 2-(diethylphosphono)isovaleronitrile (8.72 g, 40 mmol) in toluene (75 ml) was gradually added a 0.5 M solution of potassium bis(trimethylsilyl)amide in toluene (75 ml) with stirring at -70° C. under argon atmosphere. The cooling bath was removed, and the reaction mixture was stirred at room temperature for 30 minutes. The reaction mixture was cooled to -70° C. again, and farnesol (5.88 g, 26.7 mmol) was added thereto with stirring, and the mixture was allowed to warm to room temperature. After addition of water, the organic layer was separated, washed with saturated aqueous sodium bicarbonate and then saturated aqueous sodium chloride, and dried over MgSO4. The organic layer was separated from MgSO4 by filtration and concentrated to give a residue, which was purified with silica gel column chromatography (solvent: n-hexane/ethyl acetate=100:1) to obtain the aimed 2 -(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenenitrile (7.23 g, 96%; 2Z:2E=25.6:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05245085
Source datasetuspto-grants-1993_09
ORD IDord-d891efc28e36422aa4bc843ada73ddc3
Source noteuspto-grants-1993_09