HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4S,5S)-4-(1,3-dioxolan-2-yl)-5-(hydroxymethyl)dihydrofuran-2(3H)-one → (2S,3S)-3-[1,3]dioxolan-2-ylpentane-1,2,5-triol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4S,5S)-4-(1,3-dioxolan-2-yl)-5-(hydroxymethyl)dihydrofuran-2(3H)-one | HCID 11116788 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2S,3S)-3-[1,3]dioxolan-2-ylpentane-1,2,5-triol | HCID 69747925 | — |
Reaction Steps
To a solution of lithium aluminum hydride (76 mg, 1.98 mmols) in THF (10 ml) at 0° C. was added dihydrofuranone 15 (275 mg, 1.46 mmol) in THF (30 mL) dropwise. Upon completion of the reduction after 4 hours, the reaction was quenched with a saturated aqueous sodium sulfate solution at 0° C. The solvent then was decanted and the remaining residue was washed with THF (3×), EtOAc (3×), and CHCl3 (3×). The organic extracts were combined and the solvent was removed under reduced pressure, yielding a crude (2S,3S)-3-[1,3]dioxolan-2-ylpentane-1,2,5-triol, which was immediately used in the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06919465B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-54c6cd1922184409b4fa207ad6d0215d |
| Source note | uspto-grants-2005_07 |