HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Hydroxide → Lithium (RS)-alpha-(Hydroxymethyl)-3,5-bis(trifluoromethyl)benzeneacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | (RS)-Methyl alpha-(Hydroxymethyl)-3,5-bis(trifluoromethyl)benzeneacetate | HCID 21955325 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | Lithium (RS)-alpha-(Hydroxymethyl)-3,5-bis(trifluoromethyl)benzeneacetate | HCID 86760236 | 176.5% |
Reaction Steps
Lithium hydroxide (168 mg, 4 mmol) in water (2 mL) was added to a solution of (RS)-methyl α-(hydroxymethyl)-3,5-bis(trifluoromethyl)benzeneacetate (Description 7, 500 mg, 1.6 mmol) in methanol (4 mL). Methanol (2 mL) and tetrahydrofuran (2 mL) were added and the mixture was stirred at room temperature for 2 hours. The solvent was evaporated under reduced pressure and the residue was dried azeotropically by evaporating toluene (×2) to to give the crude title compound as a colorless gum (870 mg), which was used without further purification. 1H NMR (400 MHz, CD3OD) δ 3.73–3.79 (1H, m), 3.85–3.92 (1H, m), 4.02–4.06 (1H, m), 7.80 (1H, s) and 7.98 (2H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07105507B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-f2c5b4d84226488995abe2818aa3d800 |
| Source note | uspto-grants-2006_09 |