Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231269Generated: October 26, 2026

Methyl iodide → 1-Benzyl-2-methyl-3-(12cyclohexyldodecyl)glycerine

https://huagongshe.com/reaction/231269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant1-Benzyl-3-(12-cyclohexyldodecyl)glycerineHCID 53942235—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-2-methyl-3-(12cyclohexyldodecyl)glycerineHCID 20034853—

Reaction Steps

In 70 ml of tetrahydrofuran is suspended 0.86 g of sodium hydride, to which a solution of 10.2 g of 1-benzyl-3-(12-cyclohexyldodecyl)glycerine in 50 ml of tetrahydrofuran is added dropwise at room temperature with stirring. After 40 minutes stirring at room temperature, 5.11 g of methyl iodide is added and the mixture is further stirred for 2 hours. The solvent is then distilled off under reduced pressure and the residue is extracted with hexane. The extract layer is washed with water, dried and concentrated to obtain crude 1-benzyl-2-methyl-3-(12cyclohexyldodecyl)glycerine which in turn is dissolved in a mixed solvent consisting of 100 ml of ethanol and 30 ml of acetic acid. The solution is shaked in the presence of 10% palladium-carbon under hydrogen streams. The catalyst is removed by filtration and the filtrate is concentrated to obtain 9.6 g of the captioned compound as a crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04845219
Source datasetuspto-grants-1989_07
ORD IDord-b6661016ef73458b8dd179734ef0b60f
Source noteuspto-grants-1989_07