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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266431Generated: November 2, 2026

Sodium Acetate → HCID 68781569, compound

https://huagongshe.com/reaction/2266431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
Reactant1-(tert-Butyldimethylsilyloxy)-1-methoxyetheneHCID 4564491—
ReactantHCID 86631429HCID 86631429—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
CatalystTris(dibenzylideneacetone) dipalladiumHCID 9832798—
SolventDimethylformamideHCID 6228—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 68781569HCID 68781569—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of trifluoromethanesulfonic acid 3-(4-chlorobenzyl)-2,4,7-trimethylquinolin-5-yl ester (0.39), 1-(tert-butyldimethylsilyloxy)-1-methoxyethene (0.95 mL), sodium acetate (0.086 g), tris(dibenzylideneacetone) dipalladium (0) (0.080 g) and 1,1′-bis(diphenylphospino) ferrocene (0) (0.048 g) in N,N-dimethylformamide (3.0 mL) was heated by microwave irradiation at 120° C. for 10 minutes. The mixture was diluted with saturated aqueous ammonium chloride solution and extracted with ethyl acetate. The combined extracts were dried over sodium sulfate and the solvent removed under reduced pressure. Purification of the residue by column chromatography on silica gel, eluting with a mixture of ethyl acetate and cyclohexane (1:1 by volume) gave title compound, 0.11 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858640B2
Source datasetuspto-grants-2010_12
ORD IDord-e5da96efa925471fbb246cd577aa972b
Source noteuspto-grants-2010_12