HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585716Generated: October 31, 2026
Tetrabutylammonium Fluoride → HCID 178525696, compound
https://huagongshe.com/reaction/585716
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 54314967 | HCID 54314967 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178525696 | HCID 178525696 | 89.4% |
Reaction Steps
Tetrabutylammonium fluoride (0.12 ml) was added to a stirred solution of 4-(2,4-bis{[tert-butyl(dimethyl)silyl]oxy}phenyl)cyclohexanecarboxylic acid (22 mg) in tetrahydrofuran (1 ml) at room temperature under argon. After 24 hr, the reaction mixture was partitioned between ethyl acetate (30 ml) and water (30 ml). The layers were separated and the aqueous layer was extracted with ethyl acetate (2×30 ml). The combined organic extracts were dried over magnesium sulfate and evaporated in vacuo. The residue was purified by flash column chromatography (SiO2, ethyl acetate/petrol, 7:1 v/v, <1% acetic acid) to give the title compound as an orange solid (10 mg, 89%). δH (CD3OD) 1.40-1.65 (4H, m), 1.88-1.95 (2H, m), 2.06-2.14 (2H, m), 2.35 (1H, tt), 2.82 (1H, tt), 6.25-6.30 (2H, m), 6.90 (1H, m), 6.90 (1H, d); m/z (ES−) 235 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06933319B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-02e8eff9cbdd4a058872b55957f04226 |
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| Source note | uspto-grants-2005_08 |
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