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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296023Generated: October 31, 2026

Ethyl Acetate → HCID 58910060, compound

https://huagongshe.com/reaction/1296023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantStannane, tributyl(1-ethoxyethenyl)-HCID 619414—
ReactantHCID 22929833HCID 22929833—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductHCID 58910060HCID 5891006065.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

Tributyl(1-ethoxyvinyl)tin (7.77 g, 21.52 mmol) and Pd(PPh3)4 (1.18 g, 1.02 mmol) were added to a solution of the 5-bromo-1-(tert-butyl)-3-ethoxy-2-(methoxymethoxy)benzene (6.5 g, 20.4 mmol) in toluene (68 ml) and the mixture was stirred at 100° C. for 18 hours. The reaction mixture was cooled to room temperature, ethyl acetate was added, the mixture was washed with 20% aqueous KF and filtered through celite, and the organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. A 1 N HCl aqueous solution (15 ml) was added to a solution of the residue in methanol (80 ml), and the mixture was stirred at room temperature for 2 hours. Saturated sodium hydrogencarbonate solution was added to be basic and extraction was performed with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (solvent: n-hexane-ethyl acetate) to yield the title compound (3.17 g) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244730B2
Source datasetuspto-grants-2007_07
ORD IDord-f4728fdd5d8f40fa82e24ebba97c00d1
Source noteuspto-grants-2007_07