HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 3-acetyl-3-[(E,15R,16S)-16-amino-15,17-dihydroxyheptadec-13-enyl]pentane-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sphingosine | HCID 5280335 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 3-acetyl-3-[(E,15R,16S)-16-amino-15,17-dihydroxyheptadec-13-enyl]pentane-2,4-dione | HCID 129632872 | — |
Reaction Steps
In a procedure similar to Grode and Cardellina D-erythro-sphingosine (4, 2 mg, 6.7 μmol, Sigma) in acetic anhydride (1 ml) and pyridine (2 ml) was stirred at 25° C. for 4.5 h, at which time no starting material could be observed by TLC. The solvent was removed by a stream of nitrogen to give 133: white solid; silica TLC Rf 0.86 (3:12:2:2 CHCl3/1-BuOH/AcOH/H2O, phosphomolybdic acid), 0.65 (9:1 CHCl3/MeOH, phosphomolybdic acid); FABMS m/z 580, 426, 366, 306, 264; CIMS m/z 468, 454, 426, 424, 394, 366, 364, 306, 264, 144, 85, 84, 83, 61.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06800661B1 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-c9688505a00d4af3aa247ea2c20b8b7a |
| Source note | uspto-grants-2004_10 |