HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615584Generated: November 4, 2026
Tetrabutylammonium Fluoride → HCID 68182914, compound
https://huagongshe.com/reaction/1615584
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 68182917 | HCID 68182917 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68182914 | HCID 68182914 | 61.1% |
Reaction Steps
6-(morpholin-4-yl)-4-(2-naphthyl)-2-{[2-(trimethylsilyl)ethoxy]methyl}-3,4-dihydro-2H-thieno[3,2-e][1,2]thiazin-4-ol 1,1-dioxide (0.030 g, 0.055 mmol) was dissolved in THF (2.0 mL) and 1.00 M tetra-n-butylammonium fluoride in THF (0.549 mL, 0.549 mmol) was added. The solution was stirred at 40° C. overnight. The solvent was evaporated and the residue was purified using silica gel chromatography (12 g silica gel column, gradient 20% EA in hexane to 100% EA over 15 minutes) to give the product (14 mg, 55%). LCMS (FA) ES+: 417. 1H NMR (400 MHz, CD3OD) δ 7.94 (s, 1H), 7.86-7.83 (m, 3H), 7.50-7.47 (m, 2H), 7.39-7.36 (m, 1H), 5.66 (s, 1H), 5.48 (s, 1H), 3.96 (d, 1H), 3.73-3.70 (m, 4H), 3.62 (d, 1H), 3.09-3.05 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08765746B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-e5a00815dd9d46e8ba4c3da5f8e4371c |
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| Source note | uspto-grants-2014_07 |
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