HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467934Generated: October 31, 2026
Potassium Carbonate → 4-(hydroxymethyl)-2-(trifluoromethyl)benzoic Acid
https://huagongshe.com/reaction/467934
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(Bromomethyl)-2-(trifluoromethyl)benzoic acid | HCID 59563485 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(hydroxymethyl)-2-(trifluoromethyl)benzoic Acid | HCID 11096126 | 89.5% |
Reaction Steps
To a suspension of 4-bromomethyl-2-trifluoromethyl-benzoic acid (Example I7) (13.03 g) in water (200 ml) was added potassium carbonate (31.1 g). The reaction mixture was stirred at 95° C. for 1 hour. The reaction mixture was then allowed to cool to ambient temperature and was quenched by addition of aqueous hydrochloric acid (5M) (250 ml). The mixture was extracted with ethyl acetate (3×150 ml). The extracts were dried over sodium sulfate and concentrated. The residue was crystallized from ethyl acetate and heptane to give 4-hydroxymethyl-2-trifluoromethyl-benzoic acid (9.07 g) as a white crystalline powder. 1H-NMR (DMSO-d6, 400 MHz): 13.5 (br s, 1H), 7.81-7.66 (m, 3H), 5.53 (s, 1H), 4.62 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08623896B2 |
|---|
| Source dataset | uspto-grants-2014_01 |
|---|
| ORD ID | ord-0e77d6e2ad4447e6a46dda4d69265b26 |
|---|
| Source note | uspto-grants-2014_01 |
|---|