HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2,4-Bis(trifluoromethyl)phenylacetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2,4-Bis(trifluoromethyl)benzonitrile | HCID 2736117 | — |
| Product | 2,4-Bis(trifluoromethyl)phenylacetic acid | HCID 2736172 | — |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
2,4-Bis(trifluoromethyl)benzonitrile (41.5 mmol, 10.51 g) was taken up in 100 mL acetic acid, 50 mL conc. H2SO4, and 20 mL water. This was heated to 120° C. for 3 h. The reaction was then diluted with 1 L ice water, and extracted with 2×300 mL ethyl acetate. The combined organics were washed with 2×200 mL water, dried with brine and Na2SO4, and evaporated under reduced pressure. The residue was taken up in a minimum of diethyl ether and crystallized by adding sufficient hexane to precipatate the product. The solid was collected to give 7.74 g of 2,4-bis(trifluoromethyl) phenyl acetic acid as white crystals, 68.5%. NMR 1H (CDCl3) δ 7.93 (s, 1H), 7.80 (d, J=7.9 Hz,1H), 7.55 (d, J=7.9 Hz, 1H), 3.94 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05633251 |
| Source dataset | uspto-grants-1997_05 |
| ORD ID | ord-6d72a2c9c9c844b7b0c5df8ca422b9cd |
| Source note | uspto-grants-1997_05 |