Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177730Generated: October 31, 2026

Lithium Chloride → Methyl 3-acetyl-6-(benzenesulphonylmethyl)-2-methoxybenzoate

https://huagongshe.com/reaction/2177730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium ChlorideHCID 433294—
ReactantStannane, tributyl(1-ethoxyethenyl)-HCID 619414—
ReactantMethyl 6-(benzenesulfonylmethyl)-3-bromo-2-methoxybenzoateHCID 66685730—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 3-acetyl-6-(benzenesulphonylmethyl)-2-methoxybenzoateHCID 67107631—

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of methyl 6-(benzenesulphonylmethyl)-3-bromo-2-methoxybenzoate (Intermediate 65, 1.0 g), 1-ethoxyvinyl tributyl stannane (0.9 ml), tetrakis-(triphenylphosphine) palladium (0.29 g) and lithium chloride (1.0 g) in dioxane (15 ml) was stirred and heated in the microwave at 150° C. for 15 minutes. The solution was filtered and the filtrate was diluted with 1M hydrochloric acid and then stirred at room temperature for 5 hours. The resultant mixture was extracted with DCM, dried (MgSO4) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 0-75% to give methyl 3-acetyl-6-(benzenesulphonylmethyl)-2-methoxybenzoate (0.965 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067905B2
Source datasetuspto-grants-2015_06
ORD IDord-9e469a49cc35437c80c570a18a911ca6
Source noteuspto-grants-2015_06