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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290736Generated: October 30, 2026

Methanol → Dioleylamine

https://huagongshe.com/reaction/1290736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 86752565HCID 86752565—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductDioleylamineHCID 11214516—

Reaction Steps

A solution of N-oleoyloleylamide (prepared above) in THF (100 mL) was warmed to 40° C. Lithium aluminum hydride was slowly added until violent evolution of gas ceased. The reaction mixture was heated to reflux for one hour and then cooled to room temperature. Methanol (100 mL) was slowly added, followed by water (200 mL). Methylene chloride was added and the resultant suspension was stirred for fifteen minutes. The slurry was filtered and the precipitate was washed with ethanol.backslash.methylene chloride (50:50, 50 mL, 2×). The combined filtrates were washed with methylene chloride. The organic fraction was dried over magnesium sulphate, filtered and the solvent was removed under vacuum. The residue was passed down a silica gel column (150 g) using 5% methanol in methylene chloride as the eluent, to provide dioleylamine as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753613
Source datasetuspto-grants-1998_05
ORD IDord-adf58a9581914cde8f40b1475acc9572
Source noteuspto-grants-1998_05