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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431001Generated: November 2, 2026

Potassium Carbonate → Methyl 3-benzyloxy-5-phenylbenzoate

https://huagongshe.com/reaction/1431001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPhenylboronic AcidHCID 66827—
ReactantMethyl 3-benzyloxy-5-(trifluoromethanesulfonyloxy)benzoateHCID 18945283—
ReactantOxolane--water (1/1)HCID 21881883—
CatalystHCID 178418397HCID 178418397—
SolventDiethyl EtherHCID 3283—
ProductMethyl 3-benzyloxy-5-phenylbenzoateHCID 1894531590.8%

Reaction Conditions

Temperature130 °C

Reaction Steps

To a mixture of THF/H2O (5 mL, v/v=4:1) in a microwave vial was added 3-benzyloxy-5-trifluoromethanesulfonyloxy-benzoic acid methyl ester (100 mg, 0.256 mmol), phenylboronic acid (34 mg, 0.281 mmol), potassium carbonate (71 mg, 0.512 mmol), and Pd(PPh3)4 (15 mg, 0.02 mmol). The reaction vessel was sealed and subjected to microwave heating for 5 min at 130° C. After cooling, it was diluted with diethyl ether and washed with brine, dried (MgSO4), and evaporated. The residue was subjected to chromatography on silica gel using an ethyl acetate-hexane gradient to afford 74 mg (90%) of 5-benzyloxybiphenyl-3-carboxylic acid methyl ester: LCMS m/z=319.4 [C21H18O3+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940927B2
Source datasetuspto-grants-2015_01
ORD IDord-792c66f82eed4a06b8ff532e1d0997ab
Source noteuspto-grants-2015_01