Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190951Generated: November 2, 2026

Toluene → 1-(dimethylamino)-4-((9Z,12Z)-octadeca-9,12-dienyloxy)butan-2-ol

https://huagongshe.com/reaction/2190951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium hydrideHCID 24758—
Reactant3-(Dimethylamino)-1,2-propanediolHCID 79078—
ReactantLinoleyl methanesulfonateHCID 59753235—
Product1-(dimethylamino)-4-((9Z,12Z)-octadeca-9,12-dienyloxy)butan-2-olHCID 58332262—

Reaction Steps

A toluene (10 mL) solution of 3-(dimethylamino)-1,2-propanediol (98%, 1.00 g, 8.39 mmol, 1.0 equiv)) was carefully added dropwise to a toluene suspension (5 mL) of NaH (60%, 0.34 g, 8.39 mmol, 1.0 equiv) at 0° C. under argon and the resultant was stirred for 15 minutes. A toluene solution (5 mL) of linoleyl methanesulfonate (2.87 g, 8.39 mmol, 1.0 equiv) was added dropwise to the stirring mixture and the reaction was then stirred for 18 hours at 90° C. The mixture was then cooled to room temperature and quenched by the slow addition of ethanol (10 mL). The mixture was concentrated and the residue was taken up with deionized water (20 mL) and extracted three times with EtOAc (30 mL). The combined organic extracts were washed with deionized water (20 mL), dried (MgSO4), filtered, and concentrated. Chromatographic purification of the residue (0-5% MeOH in chloroform) provided 1-(dimethylamino)-4-((9Z,12Z)-octadeca-9,12-dienyloxy)butan-2-ol, a thick, clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324410B2
Source datasetuspto-grants-2012_12
ORD IDord-6d314364cb9c49f9883d7be29dc1eb62
Source noteuspto-grants-2012_12