HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175313Generated: October 30, 2026
HCID 87557856, compound → HCID 59557700, compound
https://huagongshe.com/reaction/1175313
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 87557856 | HCID 87557856 | — |
| Reactant | HCID 178506350 | HCID 178506350 | — |
| Solvent | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Product | HCID 59557700 | HCID 59557700 | — |
Reaction Steps
The solution of 5-chloro-4-(4-ethylbenzyl)-2-((2S,3S,4R,5R,6R)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)tetrahydro-2H-pyran-2-yl)phenethyl methanesulfonate (58 mg, 0.066 mmol) in 0.8 mL of 1.5 M CF3CH2ONa in CF3CH2OH was stirred at 60° C. under argon. After it was stirred for about 9 h, an additional 0.6 mL of 1.5 M of CF3CH2ONa in CF3CH2OH was added and the mixture was stirred for another 15 h at 60° C. After removal of the volatiles with a rotary evaporator under vacuum, the residue was partitioned between water and EtOAC. The organic layer was separated, washed with brine and dried over Na2SO4. Concentration gave the crude product, which was purified by preparative TLC to yield 30 mg of title compound. MS ESI (m/z) 896 (M+NH4)+, calc. 878.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07838498B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-674b9a1edf364cbd8b11140abf1d45f3 |
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| Source note | uspto-grants-2010_11 |
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