HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Hydroxide → (S)-3-(4-(3,4-Bis(trifluoromethoxy)benzyloxy)phenyl)-3-(isoxazol-3-yl)propanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-(Bromomethyl)-1,2-bis(trifluoromethoxy)benzene | HCID 45156697 | — |
| Reactant | (S)-4-Benzyl-3-((S)-3-(4-hydroxyphenyl)-3-(isoxazol-3-yl)propanoyl)oxazolidin-2-one | HCID 57801829 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-3-(4-(3,4-Bis(trifluoromethoxy)benzyloxy)phenyl)-3-(isoxazol-3-yl)propanoic acid | HCID 24898112 | 18.4% |
Reaction Steps
Cesium carbonate (137 mg, 0.4 mmol) was added to a mixture of 4-(bromomethyl)-1,2-bis(trifluoromethoxy)benzene 22.1 (71 mg, 0.21 mmol) and 7.5 (82 mg, 0.21 mmol) in DMF (2 mL). The mixture was stirred at room temperature for 16 hours. To the reaction mixture was added LiOH in water (0.5 mL, 1N solution) and THF (1 mL). The mixture was stirred at 23° C. for 3 hours. The mixture was filtered and purified by reverse phase HPLC to give 22 (19 mg) after lyophilization. MS ESI (pos.) m/e 492.1 (M+H). 1H NMR (400 MHz, CDCl3) δ 8.31 (1H, s), 7.45 (1H, s), 7.39 (2H, s), 7.21 (2H, d, J=8.3 Hz), 6.93 (2H, d, J=8.8 Hz), 6.08 (1H, s), 5.05 (2H, s), 4.57 (1H, t, J=7.6 Hz), 3.37 (1H, dd, J=16.6, 7.8 Hz), 3.00 (1H, dd, J=16.6, 7.8 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07714008B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-48dd3a8948d44d5d8fbd5b53ce384cbb |
| Source note | uspto-grants-2010_05 |