HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 85877287, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86706083 | HCID 86706083 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 85877287 | HCID 85877287 | 84.1% |
Reaction Steps
Ethyl 5-acetyl-1,3-dioxane-5-carboxylate (2) (22.3 g, 0.11 mol) was dissolved in ethanol (100 mL) and sodium borohydride (2.08 g, 0.055 mol) was added at 0° C. in portions. The mixture was stirred at the same temperature for 1 h. The excess of sodium borohydride was destroyed with acetone and the solution was extracted with ethyl acetate (3×600 mL). The combined organic extracts were concentrated in vacuo to give the title compound (18.9 g, 84%) as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09062092B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-02d4ad1173de45eb84d325529e9fa9e2 |
| Source note | uspto-grants-2015_06 |