HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809446Generated: October 30, 2026
Tetrabutylammonium Fluoride → HCID 56603201, compound
https://huagongshe.com/reaction/1809446
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 59268004 | HCID 59268004 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 56603201 | HCID 56603201 | 41% |
Reaction Steps
To a solution of 0.12 g (0.19 mmol) of N-{3-[2-(tert-butyl-diphenyl-silanyloxy)-1,1-dimethyl-ethyl]-isoxazol-5-yl}-2-methyl-2-(4-oxo-cyclohexylmethanesulfonyl)-propionamide in THF (2 mL) is added tetrabutylammonium fluoride (0.65 mL, 0.65 mmol, 1M solution in THF) and the reaction is stirred at room temperature for 48 h. The reaction mixture is quenched by addition of saturated aqueous NH4Cl solution (5 mL) and the mixture is extracted with DCM (8 mL×3). The combined organic extracts are washed with brine (10 mL), dried (MgSO4) and filtered. The filtrate is concentrated under reduced pressure and the residue purified twice by column chromatography (silica, eluent: DCM, 20% ethyl acetate, then DCM, 10% ethyl acetate) to afford 0.03 g of N-[3-(2-hydroxy-1,1-dimethyl-ethyl)-isoxazol-5-yl]-2-methyl-2-(4-oxo-cyclohexylmethanesulfonyl)-propionamide. Yield: 41%, ES-MS: 401 [M+H]
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362039B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-5fcb984f69544ce2a96c054ee109a58a |
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| Source note | uspto-grants-2013_01 |
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