Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325803Generated: October 30, 2026

Methanol → 2-Hydroxybenzene-1-sulfonamide

https://huagongshe.com/reaction/325803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBoron tribromideHCID 25134—
Reactant2-Methoxybenzene-1-sulfonamideHCID 4739144—
SolventDichloromethaneHCID 6344—
Product2-Hydroxybenzene-1-sulfonamideHCID 63754669.6%

Reaction Steps

22.2 ml of boron tribromide are added dropwise, under nitrogen and at room temperature, over 15 minutes to a suspension of 39 g of 2-methoxyphenylsulfonamide in 210 ml of dry methylene chloride. The reaction mixture is then stirred for 1 hour at room temperature. After the mixture has been cooled to 0° C., 200 ml of methanol are added over 15 minutes and the clear solution is concentrated. The oily residue is taken up in ethyl acetate and the solution is washed twice with water, dried over sodium sulfate, and evaporated to dryness. The residue is triturated with petroleum ether, affording 25.1 g of 2-hydroxyphenylsulfonamide with a melting point of 136°-138° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04443245
Source datasetuspto-grants-1984_04
ORD IDord-86c2e4da944b443f8b5d878f4cdf5054
Source noteuspto-grants-1984_04