HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218995Generated: October 26, 2026
Tetrabutylammonium Fluoride → 2-Oxazolidinone, 5-(2,2-diMethyl-4H-1,3-benzodioxin-6-yl)-3-[6-(2-hydroxyethoxy)hexyl]-, (5R)-
https://huagongshe.com/reaction/218995
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | (5R)-3-[6-(2-([tert-butyl(dimethyl)silyl]oxy}ethoxy)hexyl]-5-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-1,3-oxazolidin-2-one | HCID 46831954 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Oxazolidinone, 5-(2,2-diMethyl-4H-1,3-benzodioxin-6-yl)-3-[6-(2-hydroxyethoxy)hexyl]-, (5R)- | HCID 46831955 | 91.5% |
Reaction Steps
A solution of (5R)-3-[6-(2-{[tert-butyl(dimethyl)silyl]oxy}ethoxy)hexyl]-5-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-1,3-oxazolidin-2-one (0.79 g) in THF (30 ml) was treated with tetrabutylammonium fluoride on silica gel (3.08 g) and the mixture stirred under nitrogen at 20° C. for 2.75 h. The reaction mixture was filtered and the filtrate evaporated in vacuo to give a residue which was purified by SPE on silica. Elution with dichloromethane, then EtOAc followed by solvent evaporation in vacuo gave the title compound (0.56 g). LCMS RT=3.05 min, ES+ve 394 (MH)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08198483B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-44916f30ddb746e3baf00fb121846aa6 |
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| Source note | uspto-grants-2012_06 |
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