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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238216Generated: October 30, 2026

4-Methoxybenzenesulfonyl chloride → Benzenesulfonic Acid

https://huagongshe.com/reaction/238216

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzenesulfonyl chlorideHCID 7401—
ReactantDiethanolamineHCID 8113—
SolventTetrahydrofuranHCID 8028—
ProductBenzenesulfonic AcidHCID 7371—

Reaction Steps

To a solution of 2-(2-hydroxy-ethylamino)-ethanol (7 g, 67 mmol) and 4-methoxybenzenesulfonyl chloride (40 g, 194 mmol) in THF (400 mL) KOH (100 mL, 40%) was added dropwise at 0° C., after stirring over 3 hr the mixture was filtrated and THF was evaporated in vacuo, then extracted with EtOAc (500 mL). The organic layer was washed with brine and dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified by silica gel column to afford Benzenesulfonic acid, 4-methoxy-, [[(4-methoxyphenyl)sulfonyl]imino]di-2,1-ethanediyl ester as a colorless gum (20 g, 49%). 1H NMR (DMSO-d6) δ 7.81 (d, J=4.8 Hz, 4H), 7.79 (d, J=5.2 Hz, 2H), 7.01 (d, J=4.8 Hz, 4H), 6.93 (d, J=5.2 Hz, 2H), 4.08 (t, J=6 Hz, 4H), 3.88 (s, 6H), 3.86 (s, 3H), 3.35 (t, J=6 Hz, 4H). MS (ESI) m/z (M+1)+: 615.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642609B2
Source datasetuspto-grants-2014_02
ORD IDord-aca49454d4514b68b1b1e2d467308679
Source noteuspto-grants-2014_02