Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 18700147 | HCID 18700147 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54277468 | HCID 54277468 | — |
Reaction Steps
To a stirred solution of 2-(2,2,2-trifluoroethoxy)-4-fluorobenzoic acid (2.0 g, 8.4 mmol) from Step 1 above in THF (25 mL) at 0° C. was added BH3.THF complex (25 mL of a 1.0 M solution in THF, 25 mmol). The mixture was stirred at 0° C. for 30 min and then at ambient temperature for 6 h. Aqueous NaOH (20 mL of a 4 N solution, 80 mmol) was added and the solvents were removed under reduced pressure. The residue was partitioned between EtOAc (100 mL) and water (2×50 mL). The organic phase was dried (MgSO4), filtered, and the solvent was removed under reduced pressure to give 2-(2,2,2-trifluoroethoxy)-4-fluorobenzyl alcohol as an oil (HPLC retention time=7.3 min (method A)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05968938 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-5427e6ea394a477c8e68241d0bdbaab3 |
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| Source note | uspto-grants-1999_10 |
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