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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177672Generated: October 30, 2026

Ethyl 3-ethyl-6-(4-fluorobenzenesulphonylmethyl)-2-methoxybenzoate → 3-Ethyl-6-(4-fluorobenzenesulphonyl-methyl)-2-methoxybenzoic acid

https://huagongshe.com/reaction/2177672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-ethyl-6-(4-fluorobenzenesulphonylmethyl)-2-methoxybenzoateHCID 67108051—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-Ethyl-6-(4-fluorobenzenesulphonyl-methyl)-2-methoxybenzoic acidHCID 5291429019.9%

Reaction Steps

Potassium trimethylsilanoate (0.257 g) was added to a solution of ethyl 3-ethyl-6-(4-fluorobenzenesulphonylmethyl)-2-methoxybenzoate (Intermediate 23, 0.076 g) in dry THF (10 ml). The resultant mixture was stirred at room temperature for 3 days. The mixture was diluted with water and washed with ethyl acetate. The aqueous layer was acidified by careful addition of concentrated hydrochloric acid and then extracted with ethyl acetate, washed with water, dried (MgSO4) and filtered. The filtrate was evaporated to dryness and the residue was purified by preparative HPLC (C18), eluting with a mixture of methanol and water containing 0.1% formic acid with a gradient of 50-80% to give 3-ethyl-6-(4-fluorobenzenesulphonyl-methyl)-2-methoxybenzoic acid (0.014 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067905B2
Source datasetuspto-grants-2015_06
ORD IDord-8ea893d8768c48c4bcad1f5934d96009
Source noteuspto-grants-2015_06