HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042906Generated: October 30, 2026
Tetrabutylammonium Fluoride → HCID 67288226, compound
https://huagongshe.com/reaction/2042906
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | (2-Chloro-5-((3S,4R,5R,6R)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-tetrahydro-2H-pyran-2-yl)benzyloxy)triisopropylsilane | HCID 67287190 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67288226 | HCID 67288226 | 98% |
Reaction Steps
To a solution of (2-chloro-5-((3S,4R,5R,6R)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-tetrahydro-2H-pyran-2-yl)benzyloxy)triisopropylsilane in THF (500 mL) was added tetrabutylammonium fluoride (1.0 M in THF, 594 mL, 594 mmol) and the reaction mixture stirred at ambient temperature for 2 h. After removal of organic volatiles under reduced pressure, the residue was partitioned between EtOAc and saturated ammonium chloride. The organic layer was separated and the aqueous layer was extracted with EtOAc. The combined organic layers were washed with brine, dried over anhydrous MgSO4, filtered and concentrated in vacuo. The crude residue was purified on column chromatography to provide the titled compound (168 g, 98%, ca. 2:1 mixture of anomers (β:α)) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08586550B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-f89d59cf798e4ff1928df6e8177c816d |
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| Source note | uspto-grants-2013_11 |
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