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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408241Generated: October 27, 2026

Aluminium lithium hydride → (4E)-4-Methyl-5-(4-methylphenyl)-4-penten-1-ol

https://huagongshe.com/reaction/2408241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminium lithium hydrideHCID 21226445—
ReactantMethyl (4E)-4-methyl-5-(4-methylphenyl)-4-pentenoateHCID 58390609—
SolventTetrahydrofuranHCID 8028—
Product(4E)-4-Methyl-5-(4-methylphenyl)-4-penten-1-olHCID 6733250283.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of methyl (4E)-4-methyl-5-(4-methylphenyl)-4-pentenoate (17.18 g, 0.079 mol) in dry THF (300 ml) was treated, at −78° C. under nitrogen, with solid lithium aluminum hydride (3.15 g, 0.079 mol) in one portion. After 5 minutes the cooling bath was removed and the reaction allowed to reach room temperature and then cooled to 0° C. and treated successively with water (3.15 ml), 5% aqueous sodium hydroxide (9.45 ml) and water (3.15 ml). The reaction was stirred at room temperature for 30 minutes. Anhydrous solid sodium sulfate was added (10 g) and stirring continued for 5 minutes. The solid was filtered off, rinsed with diethyl ether and solvents were removed under vacuum. The product was purified by column chromatography on silica gel (eluent: heptanes/ethyl acetate 5:1 to 1:1) followed by bulb-to-bulb distillation (120° C./0.001 mbar). 12.54 g (yield=66%) of the desired product were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815792B2
Source datasetuspto-grants-2014_08
ORD IDord-38dbb95fbcf44dbb804d8ceb7bf3e2ed
Source noteuspto-grants-2014_08