HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → [(2R,3S,4R,5R,6S)-3,4,6-triacetyloxy-5-aminooxan-2-yl]methyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 10034-20-5 | HCID 202259 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [(2R,3S,4R,5R,6S)-3,4,6-triacetyloxy-5-aminooxan-2-yl]methyl acetate | HCID 202260 | 97.5% |
Reaction Steps
To a stirred solution of (2S,3R,4R,5S,6R)-6(acetoxymethyl)-3-amino-tetrahydro-2H-pyran-2,4,5-triyl triacetate hydrochloride (250 mg, 0.65 mmol) in CH2Cl2 (5 mL) was added triethylamine (90 μL, 0.65 mmol). The solution was diluted sated aqueous NaHCO3 (20 mL), then the resulting mixture was extracted with CH2Cl2 (3×10 mL) and the combined organic extracts were dried (Na2SO4) and concentrated to give presumably (2S,3R,4R,5S,6R)-6-(acetoxymethyl)-3-amino-tetrahydro-2H-pyran-2,4,5-triyl triacetate (220 mg) which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08334310B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-e553d3cc8a5a4f659335dd9521e045bd |
| Source note | uspto-grants-2012_12 |