HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium hydroxide, monohydrate → 5-Chloro-2-(quinolin-6-yl)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | Ethyl 5-chloro-2-(quinolin-6-yl)benzoate | HCID 67253873 | — |
| Solvent | Ethanol tetrahydrofuran water | HCID 18504229 | — |
| Product | 5-Chloro-2-(quinolin-6-yl)benzoic acid | HCID 67254523 | 91% |
Reaction Steps
To a stirring solution of ethyl 5-chloro-2-(quinolin-6-yl)benzoate (0.244 g, 0.78 mmol) in 1:1:1 THF/EtOH/H2O (21 ml) at RT was added LiOH—H2O (0.164 g, 3.91 mmol). The resulting reaction mixture was stirred at RT overnight. Solvent was removed under reduced pressure and the residue was diluted with H2O (10 mL). The aqueous solution was acidified to pH˜4 with 3M HCl and extracted with EtOAc (3×30 mL). The combined organic layers were washed with brine (20 mL), dried (MgSO4) and concentrated to afford 5-chloro-2-(quinolin-6-yl)benzoic acid (0.201 g, 91% yield) as a white solid. MS (ESI) m/z: 284.0 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07790756B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-f37de7481e4f4a5db40db182df442091 |
| Source note | uspto-grants-2010_09 |