HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20027Generated: October 30, 2026
Tetrabutylammonium Fluoride → HCID 59347043, compound
https://huagongshe.com/reaction/20027
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | (4S,5S)-Tert-butyl 5-((tert-butyldimethylsilyloxy)methyl)-4-((2-chloro-6-methylpyridin-4-yl)methyl)-2,2-dimethyloxazolidine-3-carboxylate | HCID 86614126 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59347043 | HCID 59347043 | — |
Reaction Steps
(4S,5S)-Tert-butyl 5-((tert-butyldimethylsilyloxy)methyl)-4-((2-chloro-6-methylpyridin-4-yl)methyl)-2,2-dimethyloxazolidine-3-carboxylate (0.206 g, 0.425 mmol) was dissolved in THF (4 mL) and cooled to 0° C. TBAF (0.637 ml, 0.637 mmol) was added to the mixture dropwise and the reaction was stirred 1 hr and then quenched with saturated ammonium chloride and diluted with EtOAc. The layers were separated and the aqueous layer was extracted with EtOAc. The combined organic layers were washed with water, brine, dried over sodium sulfate, and concentrated. The crude material was purified by silica column chromatography (19:1 DCM/MeOH) and then reverse phase HPLC to give the title compound. MS m/z: 371.3 (100%, M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07745484B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-35450cf6fbbc4a32827d6141fd25a376 |
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| Source note | uspto-grants-2010_06 |
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