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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584255Generated: October 30, 2026

Hydrochloric Acid → HCID 58940057, compound

https://huagongshe.com/reaction/584255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(3-Bromophenyl)acrylic acidHCID 36251—
ReactantHCID 15405941HCID 15405941—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
ProductHCID 58940057HCID 58940057—

Reaction Steps

2.2 g (8.3 mmol) of 2-methoxy-3,5-di-tert-butylphenylboronic acid, 942 mg (4.15 mmol) of 3-bromocinnamic acid and 70 ml of DME were introduced into a three-necked flask under a stream of nitrogen. 11.4 ml of aqueous potassium carbonate solution (2M) were added dropwise and the reaction medium was degassed. 144 mg (0.12 mmol) of tetrakistriphenylphosphinepalladium(0) were then added and the mixture was refluxed for 20 hours. Water and ethyl acetate were added to the reaction medium and this mixture was acidified to pH 1 with hydrochloric acid. The organic phase was separated out after settling had taken place, washed with water, dried over magnesium sulfate and evaporated. The residue obtained was purified by chromatography on a column of silica eluted with a mixture of heptane and ethyl acetate (75/25). After evaporation of the solvents, 990 mg (66%) of 3-(3′,5′-di-tert-butyl-2′-methoxy-3-biphenylyl)acrylic acid having a melting point of 182°-3° C. were collected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06924388B2
Source datasetuspto-grants-2005_08
ORD IDord-6ad7cd6e679941c88827ae74165acc25
Source noteuspto-grants-2005_08