HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (2-Trimethylsilyl-4-furyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-(Trimethylsilyl)furan-3-carbaldehyde | HCID 15663251 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (2-Trimethylsilyl-4-furyl)methanol | HCID 13333558 | — |
Reaction Steps
2-Trimethylsilyl-4-furaldehyde (1.57 g, 9.35 mmol) was added to a suspension of sodium borohydride (424 mg, 11.2 mmol) in methanol (10 ml) at 0° C. After 45 minutes, most of the methanol was evaporated and the residue taken up in ethyl ether. The ethyl ether extracts were combined, washed (water), dried (magnesium sulfate) and evaporated to dryness to give an oil, which was purified by flash chromotography on silica using 30% ethyl ether/hexane to give the title alcohol as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05268387 |
| Source dataset | uspto-grants-1993_12 |
| ORD ID | ord-4c3b68022e4140e9b71f8f1fff530767 |
| Source note | uspto-grants-1993_12 |