HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660191Generated: October 31, 2026
Tetrabutylammonium Fluoride → HCID 25205716, compound
https://huagongshe.com/reaction/660191
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 57548057 | HCID 57548057 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 25205716 | HCID 25205716 | — |
Reaction Steps
To a solution of anhydrous THF (20 ml) containing 75A (0.42 g, 1.06 mmol) were added 3.18 ml (3 eq) of TBAF (1.0 M in THF) under N2. After the addition, the resulting solution was refluxed for 18 hours and subsequently concentrated in vacuo. Ethyl acetate was added and the organic layer was washed with a concentrated NaHCO3 solution, dried (Na2SO4), filtered and concentrated in vacuo. The resulting residue was purified by flash chromatography (MeOH), followed by a further purification on (25 g) SCX-2 (MeOH followed by 1 N NH3/MeOH) to afford the title compound 76A. (oil, 0.2 g, 73%). LCMS (Method A): Rt: 1.0 min, ([M+H]+=266). 1H-NMR (400 MHz, CDCl3): δ 7.54 (s, 1H), 6.36-6.31 (m, 1H), 3.49-3.46 (m, 2H), 2.75 (t, J=7 Hz, 2H), 2.64 (t, J=6 Hz, 2H), 2.47 (s, 3H), 2.43-2.38 (m, 2H), 1.55-1.49 (m, 2H), 1.35-1.23 (m, 4H), 0.85 (t, J=7 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08084473B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-952b4852a5b94d1ba7b8397ed253f65e |
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| Source note | uspto-grants-2011_12 |
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