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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | Methyl 3-benzyloxy-5-(trifluoromethanesulfonyloxy)benzoate | HCID 18945283 | — |
| Reactant | Oxolane--water (1/1) | HCID 21881883 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Methyl 3-benzyloxy-5-phenylbenzoate | HCID 18945315 | 90.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08940927B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-792c66f82eed4a06b8ff532e1d0997ab |
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| Source note | uspto-grants-2015_01 |
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