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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164642Generated: October 25, 2026

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

https://huagongshe.com/reaction/2164642

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 numberUS04505929
Source datasetuspto-grants-1985_03
ORD IDord-76d78786cedf40808e47d51e708b1537
Source noteuspto-grants-1985_03