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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425588Generated: October 28, 2026

Methyl formate → Ethyl 4-tert-butyl-5-chloro-2-ethoxybenzoate

https://huagongshe.com/reaction/2425588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl formateHCID 7865—
ReactantSodium MethoxideHCID 10942334—
Reactant4-Tert-butyl-5-chloro-2-ethoxy-1-iodobenzeneHCID 67246286—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 4-tert-butyl-5-chloro-2-ethoxybenzoateHCID 6724581380%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a degassed solution of 4-tert-butyl-5-chloro-2-ethoxy-1-iodobenzene (2.2 g, 6.4 mmol), sodium methoxide (0.52 g, 9.6 mmol) and dichlorobistriphenylphosphinepalladium (0.25 g, 0.4 mmol) in dioxane (20 mL) was added methylformate (1.2 mL, 19.4 mmol). The resulting mixture was heated in an oil bath (60° C.) for 18 h and then allowed to cool. The solution was diluted with dioxane and filtered through a plug of Celite and concentrated. Purification of the crude residue by flash chromatography over silica gel using 5-20% ethyl acetate in hexanes gave ethyl 4-tert-butyl-5-chloro-2-ethoxybenzoate (1.39 g, 80%) as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964724B2
Source datasetuspto-grants-2011_06
ORD IDord-7f24652838d440f38232ada8f530c928
Source noteuspto-grants-2011_06