HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093716Generated: October 31, 2026
Lithium Hydroxide → 2-(Methoxymethyl)-4-methyl-7-(trifluoromethyl)quinoline-3-carboxylic acid
https://huagongshe.com/reaction/2093716
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 2-(Methoxymethyl)-4-methyl-7-(trifluoromethyl)quinoline-3-carboxylic acid methyl ester | HCID 66584032 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Methoxymethyl)-4-methyl-7-(trifluoromethyl)quinoline-3-carboxylic acid | HCID 66584114 | 66% |
Reaction Steps
A 2M aq. LiOH sol. (9.3 ml) was added to a solution of 980 mg (3.1 mmol) 2-(methoxymethyl)-4-methyl-7-(trifluoromethyl)quinoline-3-carboxylic acid methyl ester in THF (25 ml) and the mixture was subsequently heated to 60° C. for 16 h. The THF was removed as far as possible in a vacuum and the obtained aqueous solution was washed with ether, the pH was set to 2 with 2M hydrochloric acid and dilution was performed with EtOAc. The organic phase was separated and washed with brine, dried over MgSO4 and concentrated in a vacuum. 612 mg (2.0 mmol, 66%) 2-(methoxymethyl)-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 | US08445512B2 |
|---|
| Source dataset | uspto-grants-2013_05 |
|---|
| ORD ID | ord-e9aa2656e1464dd9ac8f7baa4755bfef |
|---|
| Source note | uspto-grants-2013_05 |
|---|