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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702825Generated: October 26, 2026

Hydrogen Bromide → Phenol, 4-(4-(methylsulfonyl)phenoxy)-

https://huagongshe.com/reaction/1702825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantBenzene, 1-methoxy-4-(4-(methylsulfonyl)phenoxy)-HCID 514881—
SolventAcetic AcidHCID 176—
ProductPhenol, 4-(4-(methylsulfonyl)phenoxy)-HCID 51488298.9%

Reaction Steps

A solution of 37.3 g of 4-(4-(methylsulfonyl)phenoxy)-1-methoxybenzene (Example 18), 41 ml of 48% aqueous hydrogen bromide and 185 ml of glacial acetic acid was heated at reflux under nitrogen for 21 hrs. The reaction mixture was cooled and the solvent removed in vacuo. The product was collected by filtration, washed well with water and dried, which gave 35.0 g (98.9% yield) of the product. Recrystallization from aqueous ethanol gave purified 4-(4-(methylsulfonyl)phenoxy)phenol, mp 129°-130° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04349568
Source datasetuspto-grants-1982_09
ORD IDord-1acd3a1bdd854cf59d611823204970f6
Source noteuspto-grants-1982_09