HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 4-Hydroxymethyl-2-triethylsilylfuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-Furancarboxaldehyde, 5-(triethylsilyl)- | HCID 10878438 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Hydroxymethyl-2-triethylsilylfuran | HCID 15037035 | — |
Reaction Steps
Sodium borohydride (353 mg, 0.93 mmol) was added portionwise to a solution of 2-triethylsilyl-4-furaldehyde (1.64 g, 7.79 mmol) in methanol (10 ml) at 0°. After 1 hour, most of the methanol was evaporated and the residue dissolved in a minimum amount of dilute hydrochloric acid. Extraction (ethyl acetate), drying (magnesium sulfate) and evaporation gave an oil, which was purified by flash chromatography on silica using 20% ethyl ether/hexane. Fractions with Rf of about 0.07 (10% ethyl ether/hexane) gave after evaporation the title alcohol as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05387606 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-30041682b03c4af08cb5bea47c723131 |
| Source note | uspto-grants-1995_02 |