HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 19706768, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 19706767 | HCID 19706767 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19706768 | HCID 19706768 | — |
Reaction Steps
A stirred, ice-cooled solution of 2,2-difluoro-3-ethyl-3-trimethylsilyloxy-pentanal (1.45 g, 6.08 mmol) in THF (5 ml) and ethanol (15 ml) was treated with sodium borohydride (2.76 mg, 7.30 mmol). After 30 minutes the reaction mixture was partitioned between ethyl acetate and water, and the organic layer was washed with brine, dried over MgSO4 and concentrated. Flash chromatography (50 g silica gel; 10% EtOac in petroleum ether as eluant) afforded the title compound as a colourless oil, δ 0.15 (s, 9H), 1.36 (t, 6H), 2.48 (m, 1H), 3.93 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05710142 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-93eaf3dae7c34b798e8f531bbf78f1ea |
| Source note | uspto-grants-1998_01 |