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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307555Generated: November 1, 2026

Sulfuric Acid → Methyl 3'-hydroxy-2,2'-dimethylbiphenyl-4-carboxylate

https://huagongshe.com/reaction/2307555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 4-bromo-3-methylbenzoateHCID 3294148—
Reactant3-Methoxymethoxy-2-methylbenzene-1-boronic acidHCID 22606935—
CatalystHCID 178418397HCID 178418397—
SolventMethanolHCID 887—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventDiethylether waterHCID 21584184—
ProductMethyl 3'-hydroxy-2,2'-dimethylbiphenyl-4-carboxylateHCID 22606889—

Reaction Conditions

Temperature80 °C

Reaction Steps

1.03 g (5.2 mmol) of 3-methoxymethoxy-2-methylbenzene-1-boronic acid, 1 g (4.4 mmol) of methyl 4-bromo-3-methylbenzoate and 4.4 mL of 2.0M potassium carbonate solution are dissolved in 20 mL of ethylene glycol dimethyl ether. The mixture is degassed using a stream of nitrogen for 10 minutes, and 250 mg (0.22 mmol) of tetrakis(triphenylphosphine)palladium are then added and the medium is stirred for 24 hours at 80° C. After cooling and the usual treatment, the residue obtained is dissolved in 30 mL of methanol and 0.5 mL of sulphuric acid is added. The medium is stirred at room temperature for 6 hours and then poured into an ethyl ether/water mixture. After extraction with ether, the residue is purified by chromatography on silica gel (eluent: 9 heptane/1 ethyl acetate). The desired product is obtained in the form of a thick, colourless oil (m=890 mg; Y=79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06831106B1
Source datasetuspto-grants-2004_12
ORD IDord-272dd39cc4c44f76a70ca4c98183a909
Source noteuspto-grants-2004_12