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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | Stannane, tributyl(1-ethoxyethenyl)- | HCID 619414 | — |
| Reactant | Methyl 6-(benzenesulfonylmethyl)-3-bromo-2-methoxybenzoate | HCID 66685730 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Methyl 3-acetyl-6-(benzenesulphonylmethyl)-2-methoxybenzoate | HCID 67107631 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09067905B2 |
|---|
| Source dataset | uspto-grants-2015_06 |
|---|
| ORD ID | ord-9e469a49cc35437c80c570a18a911ca6 |
|---|
| Source note | uspto-grants-2015_06 |
|---|