HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 4-(4-Cyanophenyl)-3-methylbenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Tert-butyl 4'-cyano-2-methyl-1,1'-biphenyl-4-carboxylate | HCID 22660788 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(4-Cyanophenyl)-3-methylbenzoic acid | HCID 22660816 | — |
Reaction Steps
(Step 2) To a solution of the preceding ester (3.0 g, 10.2 mmol) in methylene chloride (75 mL) at 0° C. was added TFA (75 mL) dropwise over 10 min. The ice bath was removed and stirring continued for 1 h at rt. The mixture was concentrated on a rotary evaporator and then diluted with toluene and reconcentrated to afford 4′-cyano-2-methyl-1,1′-biphenyl-4-carboxylic acid. ESI-MS m/e 228.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06803374B2 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-894e81a012a841c3875a017c08803e03 |
| Source note | uspto-grants-2004_10 |