Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207625Generated: November 1, 2026

1,4-Dioxane → 3-Benzyloxy-4,5-difluoro-phenol

https://huagongshe.com/reaction/2207625

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantDi-tert-butyl(2',4',6'-tris(propan-2-yl)-(1,1'-biphenyl)-2-yl)phosphaneHCID 11618717—
Reactant1-Bromo-3-benzyloxy-4,5-difluorobenzeneHCID 57470601—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
SolventPotassium HydroxideHCID 14797—
Product3-Benzyloxy-4,5-difluoro-phenolHCID 8964988460%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of potassium hydroxide (2246.7 mg, 40.12 mmol) in 1,4-dioxane (5 mL) and Water (5 mL) was added 2-di-tert-butylphosphino-2′,4′,6′-triisopropylbiphenyl (212.63 mg, 0.5015 mmol). The reaction mixture was degassed with nitrogen and then treated with tris(dibenzylideneacetone)dipalladium-[0](183.54 mg, 0.2006 mmol) and 1-benzyloxy-5-bromo-2,3-difluoro-benzene [CAS: 1035155-54-4](3 g, 10.03 mmol) the reaction was then heated at 90° C. for 16 hours. The reaction was diluted with aq. KOH solution (2M, 150 mL) and EtOAc (150 mL). The aqueous was separated, and acidified to pH 1 with aq. HCl (2M). The organics were then extracted into EtOAc (150 mL). The organics were separated, washed with brine (150 mL), dried over MgSO4, filtered and concentrated in vacuo to give crude 3-benzyloxy-4,5-difluoro-phenol ˜60% pure);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376436B2
Source datasetuspto-grants-2016_06
ORD IDord-06037ff7514c44ffb229f87e1ab76e41
Source noteuspto-grants-2016_06