HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Furancarboxaldehyde, 5-(triethylsilyl)- → 4-(1-Hydroxytridecyl)-2-triethylsilylfuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Furancarboxaldehyde, 5-(triethylsilyl)- | HCID 10878438 | — |
| Reactant | HCID 178443215 | HCID 178443215 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(1-Hydroxytridecyl)-2-triethylsilylfuran | HCID 15663269 | — |
Reaction Steps
Dodecylmagnesium bromide (a 1M solution in tetrahydrofuran; 14.3 ml; 14.3 mmol) was added dropwise to a solution of 2-triethylsilyl-4-furaldehyde (2.0 g, 9.52 mmol) in THF (20 ml) at 0 degrees C. under argon. After stirring at room temperature for 2 hours, the mixture was quenched with dilute HCl and extracted with ethyl ether. Evaporation of the dried (magnesium sulfate) extracts gave an oil, which was purified by flash chromatography on silica using 30% ethyl ether/hexane to give the titled alcohol. 1HNMR (CDCl3) 0.76 (q, 6H, J=8.0 Hz), 0.88 (t, 3H, J=6.3 Hz), 0.98 (t, 9H, J=8.0 Hz), 1.25 (m, 20H), 1.62 (d, 1H, J=4.3 Hz), 1.75 (m, 2H), 4.63 (dd, 1H, J=6.6 Hz, 1.9 Hz), 6.63 (s, 1H) and 7.57 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05387606 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-66d9dbc2c7164687bd1e6c500e1c2450 |
| Source note | uspto-grants-1995_02 |