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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990599Generated: November 1, 2026

2-fluoro-5-(2-methyl-[1,3]dioxolan-2-yl)-benzenesulfonamide → 5-(2-Bromomethyl-[1,3]dioxolan-2-yl)-2-fluoro-benzenesulfonamide

https://huagongshe.com/reaction/990599

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-fluoro-5-(2-methyl-[1,3]dioxolan-2-yl)-benzenesulfonamideHCID 11021640—
ReactantPhenyltrimethylammonium bromide dibromideHCID 17977687—
SolventAcetonitrileHCID 6342—
Product5-(2-Bromomethyl-[1,3]dioxolan-2-yl)-2-fluoro-benzenesulfonamideHCID 1107831362%

Reaction Steps

A solution of 8.4 g (0.0225 mole) of phenyltrimethylammonium tribromide in 20 mL of CH3CN was added dropwise to a solution of 5.2 g (0.022 mole) 2-fluoro-5(2-methyl-[1,3]dioxolan-2-yl)-benzenesulfonamide III in 100 mL of CH3CN. The reaction was stirred at room temperature for 1 hr. The solvent was evaporated in vacuo. The residue was dissolved in EtOAc, washed with water, dried over Na2SO4 and evaporated. The residue was purified by column chromatography on silica gel eluting with CH2Cl2/Et2O::9/1 to give 4.6 g of IV (62%) as an oil. CH2Cl2/Et2O::9/1 single-spot material Rƒ 0.30.1H NMR (300 MHz CDCl3) δ: (3.68, s, 2H), (3.80,m , 2H), (4.21, m, 2H), 5.15, broad s, 2H), (7.26, t, 1H), (7.75, m, 1H), 8.15, dd, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06461822B2
Source datasetuspto-grants-2002_10
ORD IDord-8a3e9eafd05846499fd43910bc549e9c
Source noteuspto-grants-2002_10