HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1039713Generated: October 29, 2026
Tetrabutylammonium Fluoride → HCID 59347048, compound
https://huagongshe.com/reaction/1039713
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | (4S,5S)-tert-butyl 5-((tert-butyldimethylsilyloxy)methyl)-2,2-dimethyl-4-((2-methylthiazol-4-yl)methyl)oxazolidine-3-carboxylate | HCID 67270237 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59347048 | HCID 59347048 | — |
Reaction Steps
(4S,5S)-Tert-butyl 5-((tert-butyldimethylsilyloxy)methyl)-2,2-dimethyl-4-((2-methylthiazol-4-yl)methyl)oxazolidine-3-carboxylate (0.100 g, 0.219 mmol) was dissolved in THF (4 mL) and cooled to 0° C. Next, TBAF (0.547 ml, 0.547 mmol) was added 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 ethyl acetate. The combined organic layers were washed with water, brine, dried over sodium sulfate, and concentrated. Purification by column chromatography (2.5:1 Hexanes/EtOAc) afforded the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08552181B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-0ccdb60febe445299d815b88db3ee81d |
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| Source note | uspto-grants-2013_10 |
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