HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096948Generated: October 31, 2026
Potassium Phosphate, Tribasic → Methyl 3-benzyloxy-5-phenylbenzoate
https://huagongshe.com/reaction/1096948
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | Methyl 3-benzyloxy-5-(trifluoromethanesulfonyloxy)benzoate | HCID 18945283 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | Methyl 3-benzyloxy-5-phenylbenzoate | HCID 18945315 | — |
Reaction Steps
Phenylboronic acid (1.2 g), Pd(PPh3)4 (364 mg) and potassium phosphate (4 g) were added in that order to a DME (60 mL) solution of methyl 3-benzyloxy-5-{[(trifluoromethyl)sulfonyl]-oxy}benzoate (2.5 g), and stirred at 85° C. for 7 hours. The reaction liquid was filtered through Celite, concentrated under reduced pressure, and the residue was diluted with ethyl acetate, water was added to it, and extracted with ethyl acetate. The organic layer was washed with water and saturated saline water, dried with anhydrous sodium sulfate, filtered, and the solvent was evaporated away. The residue was purified through silica gel column chromatography (hexane/ethyl acetate) to obtain the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08138197B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-efe18fbcd3814819bf60a783ea75708d |
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| Source note | uspto-grants-2012_03 |
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