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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028396Generated: October 30, 2026

Water → 2-Chloro-5-methoxybenzene-1-sulfonamide

https://huagongshe.com/reaction/1028396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium HydroxideHCID 14923—
Reactant2-Chloro-5-methoxybenzene-1-sulfonyl chlorideHCID 22033536—
SolventTetrahydrofuranHCID 8028—
Product2-Chloro-5-methoxybenzene-1-sulfonamideHCID 31404295.4%

Reaction Steps

To a solution of 2-chloro-5-methoxybenzenesulfonyl chloride (2.5 g, 10.4 mmol) (i.e. the product of Step A) in tetrahydrofuran (30 mL) was added 30% ammonium hydroxide (3.0 mL, 25.7 mmol) dropwise. The reaction mixture was stirred for 15 minutes, during which time a suspension formed. To this mixture water (10 mL) was added, and the tetrahydrofuran was evaporated under reduced pressure to leave an aqueous suspension of a tan solid. The solid was isolated by filtration and washed with water to afford 2.2 g of the title compound. 1H NMR (CDCl3) δ 7.63 (d, 1H), 7.43 (d, 1H), 7.03 (d, 1H), 5.13 (br s, 2H), 3.85 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735588B2
Source datasetuspto-grants-2014_05
ORD IDord-ccb2b26403a94118ac9e9a18068c8fc9
Source noteuspto-grants-2014_05