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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544887Generated: October 26, 2026

1,2-Dimethoxyethane → HCID 67196905, compound

https://huagongshe.com/reaction/544887

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
Reactant4-(Difluoromethoxy)benzeneboronic acidHCID 23082146—
Reactant4-fluoro-1-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyl)indole-3-carboxaldehydeHCID 71500259—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
CatalystRhodium, dicarbonyl(2,4-pentanedionato)-HCID 5377512—
SolventWaterHCID 962—
ProductHCID 67196905HCID 67196905—

Reaction Steps

A mixture solution of 4-fluoro-1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)indole-3-carboxaldehyde (350 mg) obtained in Example 25-(1), 4-(difluoromethoxy)benzeneboronic acid (399 mg), (acetylacetonato)dicarbonylrhodium(I) (37 mg) and 1,1′-bis-(diphenylphosphino)ferrocene (79 mg) in H2O (3.6 ml)-1,2-dimethoxyethane (3.6 ml) was stirred at 80° C. under argon atmosphere for 18 hours. The reaction mixture was cooled to room temperature, and thereto was added water (10 ml). The mixture was extracted with ethyl acetate (20 ml) 3 times, and the combined organic layer was dried over magnesium sulfate followed by being filtered through an aminosilane-treated silica gel pad. The filtrate was evaporated under reduced pressure to give crude 4-(difluoromethoxy)phenyl 4-fluoro-1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)indol-3-yl methanol, which was used in the subsequent step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935674B2
Source datasetuspto-grants-2011_05
ORD IDord-1d79e428b0d74a12bdcb8c1ac27f19f4
Source noteuspto-grants-2011_05