HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177681Generated: October 31, 2026
Ethyl Acetate → 6-(Benzenesulphonylmethyl)-2-ethyl-3-(furan-3-yl)benzoic acid
https://huagongshe.com/reaction/2177681
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | Methyl 6-(benzenesulphonylmethyl)-2-ethyl-3-(furan-3-yl)benzoate | HCID 67108200 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-(Benzenesulphonylmethyl)-2-ethyl-3-(furan-3-yl)benzoic acid | HCID 52913175 | 30.5% |
Reaction Steps
Lithium hydroxide monohydrate (0.075 g) was added to a solution of methyl 6-(benzenesulphonylmethyl)-2-ethyl-3-(furan-3-yl)benzoate (Intermediate 152, 0.092 g) in dioxane (1 ml) and water (1 ml) and the resultant solution was stirred and heated in the microwave at 150° C. for 4.5 hours. Ethyl acetate and water were added and the organic layer was separated, then acidified with concentrated hydrochloric acid. The mixture was extracted with ethyl aceate, dried (Na2SO4) and filtered. The filtrate was evaporated to dryness then azeotroped with toluene. The residue was triturated with ether and the solid was collected by filtration and dried to give 6-(benzenesulphonylmethyl)-2-ethyl-3-(furan-3-yl)benzoic acid (0.027 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09067905B2 |
|---|
| Source dataset | uspto-grants-2015_06 |
|---|
| ORD ID | ord-c5499c1ca6e54861a797e496ee6a37df |
|---|
| Source note | uspto-grants-2015_06 |
|---|