HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Furancarboxaldehyde, tetrahydro- → 1226507-56-7
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Furancarboxaldehyde, tetrahydro- | HCID 157568 | — |
| Reactant | (Trifluoromethyl)trimethylsilane | HCID 552549 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1226507-56-7 | HCID 61645213 | 31.3% |
Reaction Steps
According to Reference Example 8-12, by use of a 50 wt % aqueous tetrahydrofuran-3-carbaldehyde solution (1.00 g, 5.00 mmol) dissolved in tetrahydrofuran (15 mL), a 1 mol/L solution of tetrabutylammonium fluoride in tetrahydrofuran (1.00 mL, 1.00 mmol) and (trifluoromethyl)trimethylsilane (0.887 mL, 6.00 mmol), the mixture was stirred and reacted at room temperature for 1.8 hours. Then, purification by extraction gave 2,2,2-trifluoro-1-(tetrahydrofuran-3-yl)ethanol (Compound EJ) (266 mg, yield: 31%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08673908B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-a92888a5540e4cb0bc4d283205e61c92 |
| Source note | uspto-grants-2014_03 |