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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222573Generated: October 30, 2026

Potassium Hydroxide → 4-(1-Methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-phenol

https://huagongshe.com/reaction/222573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant4-(4-Bromophenyl)-1-methanesulfonyl-3,6-dihydro-2H-pyridineHCID 58111158—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
CatalystDi-tert-butyl(2',4',6'-tris(propan-2-yl)-(1,1'-biphenyl)-2-yl)phosphaneHCID 11618717—
SolventDiethyl EtherHCID 3283—
Product4-(1-Methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-phenolHCID 5793011685%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4-(4-bromo-phenyl)-1-methanesulfonyl-1,2,3,6-tetrahydro-pyridine (23.50 g, 74.32 mmol), potassium hydroxide (14.72 g, 222.95 mmol), 2-di-tert-butylphosphino-2′,4′,6′-tri-i-propyl-1,1′-biphenyl (2.52 g, 5.95 mmol) and tris(dibenzylideneacetone)dipalladium (0) (1.36 g, 1.49 mmol) is purged with nitrogen, and then deoxygenated 1,4-dioxane (150 mL) and deoxygenated water (150 mL) are added. The mixture is stirred at 100° C. for 1 h. The mixture is cooled to 23° C. and 1 M aq hydrochloric acid is added until pH 2-3. The aqueous layer is extracted with ethyl acetate. The organic layers are combined, dried over anhydrous sodium sulfate, filtered, and the solvent is removed to obtain a red solid. Diethyl ether is added and the solid is filtered to obtain 16 g of the title compound as an off-white solid. MS (m/z) 254 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207344B2
Source datasetuspto-grants-2012_06
ORD IDord-54fb6e78c2da4bf6ab8d671a417a7d04
Source noteuspto-grants-2012_06