HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-(Trimethylsilyl)furan-3-carbaldehyde → 3-(1-Hydroxytridecyl)-5-trimethylsilylfuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-(Trimethylsilyl)furan-3-carbaldehyde | HCID 15663251 | — |
| Reactant | HCID 178443215 | HCID 178443215 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(1-Hydroxytridecyl)-5-trimethylsilylfuran | HCID 15663268 | — |
Reaction Steps
A solution of 5-trimethylsilyl-3-furaldehyde (0.5 g, 2.97 mmol) in tetrahydrofuran (5 ml) was added to a solution of dodecyl magnesium bromide (5.95 mmol; prepared from 1.48 g dodecyl bromide and 146 mg magnesium turnings in 30 ml tetrahydrofuran) at room temperature. After 2 hours, the mixture was quenched with ammonium chloride solution and extracted thoroughly with ethyl ether. Evaporation of the dried (magnesium sulfate) extracts gave an oil which was flash chromatographed on silica using 10% ethyl ether/hexane. Fractions with Rf about 0.13 on evaporation gave the title alcohol as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05045564 |
| Source dataset | uspto-grants-1991_09 |
| ORD ID | ord-cf2efc4d6f604938a9b3404167957f49 |
| Source note | uspto-grants-1991_09 |