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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247437Generated: October 25, 2026

Hydrochloric Acid → Methyl (3'-benzyloxy-4'-methoxybiphenyl-3-yl)acetate

https://huagongshe.com/reaction/2247437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPropylene GlycolHCID 1030—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 2-(3-bromophenyl)acetateHCID 11746402—
Reactant2-Benzyloxy-1-methoxybenzeneboronic acidHCID 68633201—
CatalystHCID 178527692HCID 178527692—
SolventDiethyl EtherHCID 3283—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductMethyl (3'-benzyloxy-4'-methoxybiphenyl-3-yl)acetateHCID 5921925555.5%

Reaction Steps

1.753 g of 2-Benzyloxy-1-methoxybenzeneboronic acid was suspended in 50 ml of diethyl ether, and 0.49 ml of propylene glycol was added thereto. The mixture was stirred at room temperature for 1 hour, and the solvent was removed to give 2-(3-benzyloxy-4-methoxyphenyl)-[1,3,2]dioxaborynane. This product was dissolved in 30 ml of 1,2-dimethoxyethane, then 1.5 g of potassium carbonate, 1.9 g of methyl 3-bromophenylacetate and 270 mg of dichlorodiphenyl phosphinoferrocene palladium were added thereto, and the mixture was stirred at 80° C. for 3 hours in a nitrogen atmosphere. The reaction mixture was neutralized with 1N hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate and then filtered, and the filtrate was concentrated. The residue was purified by silica gel column chromatography, to give 1.356 g of the title compound in the 6:1→4:1 fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687664B2
Source datasetuspto-grants-2010_03
ORD IDord-1e524e2bacc5478e973d7ae9fb5b2da0
Source noteuspto-grants-2010_03