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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042520Generated: November 1, 2026

Phosphinic Acid → 2-tert-Butyl-6-((2-methoxybiphenyl-3-yl)(phenyl)methyl)phenol

https://huagongshe.com/reaction/1042520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphinic AcidHCID 4124402—
Reactant(2-(Benzyloxy)-3-tert-butylphenyl)(2-methoxybiphenyl-3-yl)(phenyl)methanolHCID 58238509—
SolventAcetonitrileHCID 6342—
Product2-tert-Butyl-6-((2-methoxybiphenyl-3-yl)(phenyl)methyl)phenolHCID 5823851885%

Reaction Steps

A solution of 15 (1.02 g, 1.93 mmol) in acetonitrile (24 mL) was treated with 50% aqueous hypophosphorous acid (11 mL) and stirred at reflux for 1.5 hr. After cooling, the acetonitrile was removed on a rotary evaporator. The residue was diluted with water (100 mL) and extracted with ethyl acetate (150 mL). The organic layer was washed with water (100 mL), saturated sodium bicarbonate (100 mL) and water (100 mL). The organic layer was dried over sodium sulfate and stripped. The crude product was purified by chromatography on silica (60 g) with 1% ethyl acetate in hexane (2 L). The relevant fractions were stripped and the residue was taken up in ethanol (12 mL) and stirred at 60° C. on a water bath for 30 min. The resulting slurry was allowed to cool overnight. The crystals were collected by filtration, washed with cold ethanol and dried in a vacuum oven at 65° C. to produce pure B4 (0.69 g, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557936B2
Source datasetuspto-grants-2013_10
ORD IDord-d2f5cab5ffec41298694799aa1e18f8a
Source noteuspto-grants-2013_10