HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → HCID 18426311, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 23445658 | HCID 23445658 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18426311 | HCID 18426311 | 90.5% |
Reaction Steps
At ambient temperature, to a stirred solution of (2-n-butyl-benzofuran-3-yl)-(2′-[(2-methoxyethoxy)methoxy]-[1,1′;3′,1″]terphenyl-5′-yl)-methanone (0.371 g, 0.695 mmol) in CH2Cl2 (3.71 mL) was added trifluoroacetic acid (3.71 mL). After 0.5 h, the reaction was diluted with ether (50 mL), washed with H2O (3×), dried (MgSO4) and concentrated. The crude product was purified on Biotage KP-Sil eluting with 10% acetone/hexane to give 0.281 g (90%) of the title compound. 1H NMR (DMSO-d6) δ 0.77 (t, 3H), 1.22 (sextet, 2H), 1.64 (quintet, 2H), 2.87 (t, 2H), 7.29-7.65 (m, 14H), 7.66 (s, 2H), 9.39 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06451845B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-64ef1ce5e0c647f8b82f136db01e19f1 |
| Source note | uspto-grants-2002_09 |