HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723354Generated: November 2, 2026
Trifluoroacetic acid → HCID 21873402, compound
https://huagongshe.com/reaction/723354
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 4-(o-Tolyloxy)aniline | HCID 92505 | — |
| Reactant | HCID 21873475 | HCID 21873475 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 21873402 | HCID 21873402 | — |
Reaction Steps
Carbonyldiimidazole (40 mg) was added to a solution of 4-o-tolyloxyphenylamine (50 mg) in dimethylformamide (2 mL) at 0° C. After 30 minutes, (2,2-dimethoxyethyl)-[4-(2-dimethylaminoethoxy)phenyl]amine (67 mg) was added, and the mixture was heated at 80° C. for 2 hours. After cooling to room temperature, trifluoroacetic acid (0.5 mL) was added and the mixture was left to stand for 72 hours. The reaction solution was diluted with ethyl acetate and washed with saturated sodium bicarbonate solution. The organic phase was dried and concentrated. The residue was purified by preparative HPLC. The product with the molecular weight of 429.52 (C26H27N3O3); MS (ESI): 430 ([M+H]+), was obtained as hydrotrifluoroacetate in this way.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07141561B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-a46f2375f0a44419bf14d3bde4c87df0 |
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| Source note | uspto-grants-2006_11 |
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