Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175313Generated: October 30, 2026

HCID 87557856, compound → HCID 59557700, compound

https://huagongshe.com/reaction/1175313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 87557856HCID 87557856—
ReactantHCID 178506350HCID 178506350—
Solvent2,2,2-TrifluoroethanolHCID 6409—
ProductHCID 59557700HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838498B2
Source datasetuspto-grants-2010_11
ORD IDord-674b9a1edf364cbd8b11140abf1d45f3
Source noteuspto-grants-2010_11