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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Propylene Glycol | HCID 1030 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 2-(3-bromophenyl)acetate | HCID 11746402 | — |
| Reactant | 2-Benzyloxy-1-methoxybenzeneboronic acid | HCID 68633201 | — |
| Catalyst | HCID 178527692 | HCID 178527692 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | Methyl (3'-benzyloxy-4'-methoxybiphenyl-3-yl)acetate | HCID 59219255 | 55.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07687664B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-1e524e2bacc5478e973d7ae9fb5b2da0 |
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| Source note | uspto-grants-2010_03 |
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