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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2077127Generated: October 27, 2026

Sodium Iodide → 3-(4-Fluoro-phenoxy)-2-{[methoxycarbonylmethyl-(toluene-4-sulfonyl)-amino]-methyl}-benzoic acid ethyl ester

https://huagongshe.com/reaction/2077127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 2-(4-methylphenylsulfonamido)acetateHCID 562880—
Reactant2-Bromomethyl-3-(4-fluoro-phenoxy)-benzoic acid ethyl esterHCID 67110141—
SolventDimethylformamideHCID 6228—
Product3-(4-Fluoro-phenoxy)-2-{[methoxycarbonylmethyl-(toluene-4-sulfonyl)-amino]-methyl}-benzoic acid ethyl esterHCID 6711010654.1%

Reaction Steps

A mixture of 2-bromomethyl-3-(4-fluoro-phenoxy)-benzoic acid ethyl ester (3.37 g, 9.57 mmol), (toluene-4-sulfonylamino)-acetic acid methyl ester (2.33 g, 9.57 mmol), sodium iodide (2.15 g, 14.36 mmol) and potassium carbonate (1.98 g, 14.36 mmol) in anhydrous dimethylformamide (22 mL) was stirred at room temperature for 24 h before it was quenched with water, and extracted with ethyl acetate. The organic layer was washed with water, brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with a gradient of ethyl acetate and hexane to give the title compound as a yellow oil (2.67 g): MS: (+) m/z 538.13 (M+Na+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928120B2
Source datasetuspto-grants-2011_04
ORD IDord-7cb7d50a0643471eb65f34111232fecc
Source noteuspto-grants-2011_04