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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280655Generated: October 30, 2026

Sodium Carbonate → (4'-(Benzyloxy)-2,2',6'-trimethylbiphenyl-3-yl)methanol

https://huagongshe.com/reaction/2280655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant(3-Bromo-2-methylphenyl)methanolHCID 10035697—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Reactant(4-(Benzyloxy)-2,6-dimethylphenyl)boronic acidHCID 23157199—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product(4'-(Benzyloxy)-2,2',6'-trimethylbiphenyl-3-yl)methanolHCID 8970178257.2%

Reaction Steps

2-Methyl-3-bromo-phenylmethanol (201 mg, 1 mmol, prepared by a method disclosed in PCT patent application WO2010143733), (4-(benzyloxy)-2,6-dimethylphenyl) boronic acid 12b (300 mg, 1.20 mmol), 1 mL of 2M aqueous sodium carbonate solution, 2-dicyclohexylphosphino-2′,6′-dimethoxy-1,1′-biphenyl (33 mg, 0.08 mmol) and tris(dibenzylideneacetone)dipalladium (18 mg, 0.02 mmol) were dissolved in 1 mL of N,N-dimethylformamide. The reaction mixture was reacted at 120° C. under microwave conditions for 1 hour. The resulting mixture was mixed with 10 mL of water and extracted with ethyl acetate (20 mL×2). The combined organic extracts were washed with saturated sodium chloride solution (30 mL), dried with anhydrous magnesium sulphate, and filtered. The filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography with elution system B to obtain the title compound (4′-(benzyloxy)-2,2′,6′-trimethylbiphenyl-3-yl)methanol 12c (190 mg, yield 57.2%) as a red slime.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139548B2
Source datasetuspto-grants-2015_09
ORD IDord-6e7a7ffad3c14926aa54fe3ba7a43d0f
Source noteuspto-grants-2015_09