HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3,6-Trifluorobenzoic acid → 2,3,6-Trifluorobenzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3,6-Trifluorobenzoic acid | HCID 520062 | — |
| Reactant | HCID 178418435 | HCID 178418435 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,3,6-Trifluorobenzyl alcohol | HCID 145500 | 102% |
Reaction Steps
To a solution of sodium boron hydride (51.6 g) in tetrahydrofuran (500 ml) is added dropwise a solution of 2,5,6-trifluorobenzoic acid (120 g) in tetrahydrofuran (200 ml) with stirring at below 10° C., and thereto is further added dropwise a solution of BF3 ·(C2H5)2O (232 ml) in tetrahydrofuran (500 ml) under ice cooling. The mixture is stirred at room temperature overnight. The reaction mixture is poured into ice water (1.5 liter) and is extracted with diethyl ether. The extract is dried over magnesium sulfate and the solvent is distilled off under reduced pressure to give 2,3,6-trifluorobenzyl alcohol (112.7 g), as pale yellow oil, b.p. 112° C. (30 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04855292 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-a0d0a6f2d3334cd085901328c37f23f4 |
| Source note | uspto-grants-1989_08 |