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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Benzyl-3-(12-cyclohexyldodecyl)glycerine | HCID 53942235 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Benzyl-2-methyl-3-(12cyclohexyldodecyl)glycerine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04845219 |
|---|
| Source dataset | uspto-grants-1989_07 |
|---|
| ORD ID | ord-b6661016ef73458b8dd179734ef0b60f |
|---|
| Source note | uspto-grants-1989_07 |
|---|