HuagongsheHuagongshe Chemistry Print Report · For research reference only
Fluoroacetic acid → N-Fluoroacetyl sphingosine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Fluoroacetic acid | HCID 5237 | — |
| Reactant | Sphingosine | HCID 5280335 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 2-Chloro-1-methylpyridine iodide | HCID 22448423 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | N-Fluoroacetyl sphingosine | HCID 131719401 | — |
Reaction Steps
5.0 gr of sphingosine (16.70) mM), prepared according to Example 4, are reacted with 2.1 gr of the sodium salt of fluoroacetic acid (20.88 mM), in the presence of 5.3 gr of 2-chloro-1-methylpyridine iodide (20.88 mM) and 5.8 cc of triethylamine (42.00 mM) in 80 cc of dimethylformamide, at room temperature overnight. The solvent is evaporated, and the residue is gathered in CH2Cl2 and washed with H2O. It is anhydrified and purified by chromatography, eluting with a mixture of CH2 Cl2 /ethyl acetate/CH3CH 70:30:1 v/v/v.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05792858 |
| Source dataset | uspto-grants-1998_08 |
| ORD ID | ord-20ec3f5d50784080845d146b4879883b |
| Source note | uspto-grants-1998_08 |