HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736636Generated: October 29, 2026
Tetrabutylammonium Fluoride → HCID 15344101, compound
https://huagongshe.com/reaction/1736636
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 10875945 | HCID 10875945 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15344101 | HCID 15344101 | 84.4% |
Reaction Steps
A solution of 74.5 mg (0.117 mmol) of (2S,3S,5S)-2-(Boc-amino)-5-(N-((3-pyridinyl)methoxycarbonyl)amino)-1-phenyl-6-(4-pyridinyl)-3-(tert-butyldimethylsilyloxy)-hexane in 4 ml of tetrahydrofuran was treated with 102 μl of 1 M solution of tetrabutylammonium fluoride in tetrahydrofuran. After being stirred at ambient temperature for 24 h, the solvent was removed in vacuo, and the residue was purified by silica gel chromatography using 10% methanol in dichloromethane to provide 51.4 mg (84%) of the desired compound as a white solid. 1H NMR (CDCl3) δ 1.37 (s, 9H), 1.65 (t, 2H), 2.82-3.01 (m, 5H), 3.70 (m, 2H), 4.03 (m, 1H), 4.78 (d, 1H), 5.03 (s, 2H), 5.18 (br d, 1H), 7.06 (d, 2H), 7.16-7.31 (m, 6H), 7.61 (d, 1H), 8.44 (d, 2H), 8.57 (s , 2H). Mass spectrum: (M+H)+ 521.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05541320 |
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| Source dataset | uspto-grants-1996_07 |
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| ORD ID | ord-15d51cb50f1043969cd661f4fb101051 |
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| Source note | uspto-grants-1996_07 |
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