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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1950690Generated: October 30, 2026

Hydrogen Bromide → Phenol, 4-hexadecyl-

https://huagongshe.com/reaction/1950690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantTolueneHCID 1140—
Reactant1-Hexadecyl-4-methoxybenzeneHCID 14143934—
CatalystHexadecyltributylphosphonium bromideHCID 84716—
SolventWaterHCID 962—
ProductPhenol, 4-hexadecyl-HCID 75768—

Reaction Conditions

Temperature135 °C

Reaction Steps

The alkyl anisole of Example 1 (40 g) was transferred to a dry 3-neck 1-litre flask under nitrogen. To this was added tributylhexadecylphosphonium bromide (12.69 g) and HBr (48% aq., 71.4 ml). The resulting thick suspension was warmed to 135° C. and stirred for five hours. Toluene was added and the reaction was transferred to a separating funnel. The organic layer was shaken with water and then the aqueous extract shaken with fresh toluene. The organic extracts were combined and dried with MgSO4. The solvent was removed in vacuo to give the title compound as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404627B2
Source datasetuspto-grants-2013_03
ORD IDord-561e088031d9415eabe5d14cf3b3d33b
Source noteuspto-grants-2013_03