HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Hydroxide → [5-fluoro-(4-methanesulfonyl-2-trifluoromethyl-benzyl)-2-methyl-1H-indol-3-yl]-acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | [5-fluoro-(4-methanesulfonyl-2-trifluoromethyl-benzyl)-2-methyl-1H-indol-3-yl]-acetic acid ethyl ester | HCID 66936503 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [5-fluoro-(4-methanesulfonyl-2-trifluoromethyl-benzyl)-2-methyl-1H-indol-3-yl]-acetic acid | HCID 23627405 | — |
Reaction Steps
To a stirring solution of [5-fluoro-(4-methanesulfonyl-2-trifluoromethyl-benzyl)-2-methyl-1H-indol-3-yl]-acetic acid ethyl ester (28 mg, 0.06 mmol) dissolved in THF (1 ml) at room temperature, is added 2N LiOH aq (1 ml). The reaction mixture is stirred at room temperature for 2 h and partitioned between water/EtOAc (20 ml). The aqueous phase is separated and acidified with 1N HCl aq to pH 4. The product is extracted into EtOAc (20 ml), dried (MgSO4) and evaporated in vacuo; [M+H]+ 444.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07888383B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-8978a4a94ce04513ae392f56cf854f9e |
| Source note | uspto-grants-2011_02 |