HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242115Generated: October 30, 2026
Lithium Hydroxide → 2-Ethoxy-4-methyl-7-(trifluoromethyl)quinoline-3-carboxylic acid
https://huagongshe.com/reaction/242115
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 2-Ethoxy-4-methyl-7-(trifluoromethyl)quinoline-3-carboxylic acid ethyl ester | HCID 66583842 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | 2-Ethoxy-4-methyl-7-(trifluoromethyl)quinoline-3-carboxylic acid | HCID 66584048 | 95% |
Reaction Steps
2M aq. LiOH sol. (38 ml) was added to a solution of 5.1 g (15.5 mmol) 2-ethoxy-4-methyl-7-(trifluoromethyl)quinoline-3-carboxylic acid ethyl ester in a MeOH/THF mixture (in each case 38 ml) and subsequently heated to 60° C. for 16 h. The organic solvents were removed as far as possible in a vacuum and the obtained aqueous solution was washed with EtOAc, set at pH 2 with 2M hydrochloric acid and diluted with EtOAc. The organic phase was separated and washed with brine, dried over MgSO4 and concentrated in a vacuum. 4.4 g (14.7 mmol, 95%) 2-ethoxy-4-methyl-7-(trifluoromethyl)quinoline-3-carboxylic acid was obtained as a residue. The raw product was further converted without additional purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08653101B2 |
|---|
| Source dataset | uspto-grants-2014_02 |
|---|
| ORD ID | ord-7f0117f3b386454fa26c5a0e537b3351 |
|---|
| Source note | uspto-grants-2014_02 |
|---|