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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110174Generated: October 26, 2026

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

https://huagongshe.com/reaction/1110174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantOxalic AcidHCID 971—
ReactantDiisobutylaluminumhydrideHCID 21225700—
Reactant2-(1-Methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenenitrileHCID 53657145—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
Product2-(1-Methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenalHCID 5444191884%

Reaction Conditions

Temperature-70 °C

Reaction Steps

To a solution of 2-(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenenitrile (856 mg, 3.0 mmol) in n-hexane (30 ml) was added a 0.5M solution of diisobutylaluminium hydride in toluene (6 ml) with stirring at -70° C. under argon atmosphere. After one hour, water (3 ml) was added, the cooling bath was removed, and the reaction mixture was stirred well. Resultant white precipitates were filtered and washed. The filtrate was concentrated to give a residue, which was dissolved in n-hexane (10 ml). The n-hexane solution was combined with a 10% aqueous solution of oxalic acid (5 ml) and stirred for 3 hours. The organic layer was extracted and separated, washed with water, dried over MgSO4, and concentrated. The resultant residue was subjected to silica gel column chromatography (solvent: n-hexane/ethyl acetate=10:1) to obtain 2-(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenal (865 mg, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05324869
Source datasetuspto-grants-1994_06
ORD IDord-44f3e5b21991411fa403ac7f1b688cf9
Source noteuspto-grants-1994_06