HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1,2-Di-O-(n-hexadecyl)-3-O-(3-cyanobenzyl)-glycerol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Benzonitrile, 3-(bromomethyl)- | HCID 97249 | — |
| Reactant | 2,3-Bis(hexadecyloxy)propan-1-ol | HCID 102548 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,2-Di-O-(n-hexadecyl)-3-O-(3-cyanobenzyl)-glycerol | HCID 23466158 | 68% |
Reaction Steps
Sodium hydride (1.056 g. of 50 wt. % mineral oil dispersion, 22 mmoles) was added to a solution of 1,2-di-O-(n-hexadecyl)-glycerol (9.73 g., 18 mmoles) in tetrahydrofuran (150 ml.) and the resulting solution stirred for 20 minutes at room temperature under nitrogen. m-Cyanobenzyl bromide (4.0 g., 20 mmoles) was added and the reaction mixture stirred overnight at room temperature under nitrogen. Water (200 ml.) was then added cautiously and the resulting mixture extracted with ethyl acetate (3×150 ml.). The combined ethyl acetate extract was dried (MgSO4), filtered and evaporated in vacuo to an oil (12 g.), which was purified by silica gel chromatography (elution with benzene:hexane) [8.0 g., 68% yield, oil, ir (CHCl3) 2230 cm-1 ].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04193999 |
| Source dataset | uspto-grants-1980_03 |
| ORD ID | ord-7fb9b1a512fa4bd4bb58875510021a7a |
| Source note | uspto-grants-1980_03 |