HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → HCID 67279429, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | HCID 67279307 | HCID 67279307 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67279429 | HCID 67279429 | 86% |
Reaction Steps
Compound 2 (2.5 g, 3.21 mmol) was dissolved in dichloromethane (25 mL). A solution of trifluoroacetic acid and trifluoroacetic anhydride in dry dichloromethane (1.83 M; 50 mL) was added and the reaction was allowed to proceed for 15 min at RT. The mixture was cooled on ice-water bath, and it was made basic with triethylamine, poured into methanol and concentrated. Precipitation from the mixture of dichloromethane and petroleum ether gave the title compound. Yield was 86%. Mp. 90° C. 1H NMR (DMSO-d6): 7.57 (2H, d, J 8.9); 6.83 (2H, d, J 8.9); 4.81 (2H, t, J 5.8); 4.22 (1H, m); 3.54 (4H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08158782B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-443ec68430a94b13b069c96bde810f58 |
| Source note | uspto-grants-2012_04 |