HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Oleyl 2,3,4-tri-O-acetyl-1-thio-beta-L-fucopyranoside
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oleyl iodide | HCID 10894154 | — |
| Reactant | 2,3,4-tri-O-acetyl-1-thio-beta-L-fucopyranose | HCID 23238908 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Oleyl 2,3,4-tri-O-acetyl-1-thio-beta-L-fucopyranoside | HCID 70572110 | — |
Reaction Steps
A solution of 2,3,4-tri-O-acetyl-1-thio-β-L-fucopyranose (2.0 g, 6.5 mmol) and oleyl iodide (2.5 g, 6.6 mmol) in dichloromethane (40 ml) containing triethylamine (1 ml) is kept under nitrogen for 2 days at room temperature. The solution is worked up in the normal manner and the resulting syrup is column chromatographed on silica gel with 2-10% ethyl acetate in chloroform as eluents. Oleyl 2,3,4-tri-O-acetyl-1-thio-β-L-fucopyranoside is isolated as a syrup (1.2 g, 32%), [α]D +26° (c, 2.19, chloroform).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04259324 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-7f9fa20bbbb14e818172124164ac4b40 |
| Source note | uspto-grants-1981_03 |