HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oleyl p-toluenesulfonate → 1,3-O-dioleyl-2-O-tetrahydrofuranylglycerol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oleyl p-toluenesulfonate | HCID 11258749 | — |
| Reactant | 2-O-tetrahydrofuranylglycerol | HCID 19361256 | — |
| Reactant | HCID 178418922 | HCID 178418922 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 1,3-O-dioleyl-2-O-tetrahydrofuranylglycerol | HCID 70256374 | 18% |
Reaction Steps
In 30 ml of xylene was dissolved 854 mg (5.3 mmol) of 2-O-tetrahydrofuranylglycerol. To this was added 1.78 g (15.9 mmol) of t-butoxypotassium under argon gas and the mixture was stirred for 5 minutes. Then, 10 ml of a solution of 6.71 g (15.9 mmol) oleyl p-toluenesulfonate in xylene was added dropwise and the mixture was stirred under reduced pressure (20-30 mmHg) at ambient temperature for 30 minutes and further at 50° C. for 1 hour. This reaction mixture was poured in ice-water and extracted with ether, and the extract was washed with water, dried, and concentrated. The residue was purified by column chromatography (silica gel/chloroform) to provide 628 mg (18%) of 1,3-O-dioleyl-2-O-tetrahydrofuranylglycerol as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05705188 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-9357d88419b74d578cfe1241262cd1df |
| Source note | uspto-grants-1998_01 |