HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1055499Generated: November 1, 2026
Tetrabutylammonium Fluoride → HCID 118377801, compound
https://huagongshe.com/reaction/1055499
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 131736379 | HCID 131736379 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 118377801 | HCID 118377801 | 77.8% |
Reaction Steps
To a solution of tert-butyl-dimethyl-[[(2R,3R,4S,5R,6S)-3,4,5-tribenzyloxy-6-[4-chloro-3-[(4-ethoxyphenyl)methyl]phenyl]-6-methoxy-tetrahydropyran-2-yl]methoxy]silane 1f (84.1 g, 102.1 mmol) in tetrahydrofuran (400 mL) was added tetrabutylammonium fluoride (53.4 g, 204.2 mmol) at room temperature. The mixture was stirred at room temperature for 2 hours and quenched with 100 mL of saturated aqueous sodium bicarbonate. The resulting mixture was washed with water (100 mL). The aqueous layer was extracted with ethyl acetate (100 mL×3). The combined organic layers were washed with saturated aqueous sodium chloride (200 mL), dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by silica gel chromatography eluted with PE/EtOAc(v/v)=10/1 to give the title compound 1g as yellow oil (56.3 g, 77.8%). The compound was characterized by the following spectroscopic data: 1H NMR (400 MHz, CDCl3) δ (ppm): 7.34 (m, 13H), 7.25 (m, 3H), 7.04 (m, 2H), 6.99 (m, 2H), 6.77 (m, 2H), 4.90 (m, 3H), 4.69 (d, 1H), 4.49 (d, 1H), 4.16 (t, 1H), 4.10 (d, 1H), 4.00 (m, 2H), 3.98 (m, 2H), 3.81 (m, 1H), 3.70 (m, 1H), 3.68 (m, 1H), 3.66 (m, 1H), 3.29 (d, 1H), 3.06 (s, 3H), 1.75 (bs, 1H), 1.38 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09394329B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-f4cf64781d184311807adc4a10e3ab69 |
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| Source note | uspto-grants-2016_07 |
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