HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrabutylammonium Fluoride → HCID 57911451, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 57911410 | HCID 57911410 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57911451 | HCID 57911451 | — |
Reaction Steps
TBAF (0.954 mL, 0.954 mmol) was added to the THF (5 mL) solution of (E)-6-(2,5-difluorophenyl)-9-(triisopropylsilyloxy)-8,9-dihydro-7H-cyclohepta[b]pyridine (0.2049 g, 0.477 mmol) at rt. The reaction was stirred at room temperature for 6 hours. The solvent was removed via vacuum and the product was purified by flash column eluted with ethyl acetate in hexane from 0 to 50% to 100% (102.2 mg, 78%). MS (ESI)[M+H+]=274.23 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 8.37 (dd, J=4.78, 1.26 Hz, 1H) 7.51 (dd, J=7.81, 1.26 Hz, 1H) 7.17-7.27 (m, 1H) 6.87-7.05 (m, 3H) 6.44 (s, 1H) 5.74 (br. s., 1H) 4.77 (dd, J=10.45, 2.64 Hz, 1H) 2.79-2.93 (m, 1H) 2.66-2.77 (m, 1H) 2.48-2.60 (m, J=13.53, 5.45, 5.45, 2.77 Hz, 1H) 1.97-2.11 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08143403B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-1aca14d3686d4c7cb1d9064672984da3 |
| Source note | uspto-grants-2012_03 |