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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130417Generated: October 30, 2026

3-Bromoanisole → 4-Bromo-2-methoxybenzene-1-sulfonyl chloride

https://huagongshe.com/reaction/130417

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromoanisoleHCID 16971—
ReactantChlorosulfonic acidHCID 24638—
Product4-Bromo-2-methoxybenzene-1-sulfonyl chlorideHCID 18754952—

Reaction Conditions

Temperature0 °C

Reaction Steps

To chlorosulfonic acid (20 ml) at 0° C. was added dropwise 3-bromoanisole (18.7 g, 0.1 mol) at such a rate that the internal temperature remained below 5° C. The mixture was stirred at 0° C. for 1 hour and added dropwise to crushed ice. The mixture was extracted with ethyl acetate and the combined organic layers were washed with water and brine, dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue was purified by chromatography on silica gel (1:25 ethyl acetate:pentane) to afford the title compound; 4-bromo-2-(methyloxy)benzenesulfonyl chloride (D30) 1H-NMR (CDCl3) δ 7.81 (1H, d, J 8 Hz), 7.28 (1H, d, J 2 Hz), 7.26 (1H, dd, J 8, 2 Hz), 4.07 (3H, s) and an isomer; 2-bromo-4-(methyloxy)benzenesulfonyl chloride 1H-NMR (CDCl3) δ 8.12 (1H, d), 7.33 (1H, d), 6.97 (1H, dd), 3.92 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381728B2
Source datasetuspto-grants-2008_06
ORD IDord-203f0475cad0465b95fc7f337c0a8c19
Source noteuspto-grants-2008_06