HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113012Generated: October 30, 2026
2-(Methoxymethyl)benzeneboronic acid → HCID 11515794, compound
https://huagongshe.com/reaction/2113012
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Methoxymethyl)benzeneboronic acid | HCID 3759408 | — |
| Reactant | Methyl 3-((4-iodophenoxy)methyl)benzoate | HCID 57643351 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 11515794 | HCID 11515794 | — |
Reaction Steps
A solution of 3-(4-iodo-phenoxymethyl)-benzoic acid methyl ester (of intermediate 1; 37 mg, 0.1 mmol) in dioxane (2 mL) was degassed with nitrogen and then added to a reaction vial containing 2-methoxymethylphenylboronic acid (available from Apollo Scientific Ltd., Stockport, UK). The solution was sonicated and degassed and a solution of sodium hydroxide (4 M, 0.2 mL) was added, followed by bis(tri-cyclo-hexylphosphine)palladium (available from Strem Chemicals, Inc., Newburyport, Mass.; 0.005 mmol) was added. The mixture was degassed and then heated in a microwave oven at 170 degrees for 25 min. The reaction mixture was filtered through silica and the silica washed with dioxane (1 mL), and dimethylacetamide (1 mL). 1 M HCl was added until a solid formed. The vial was centrifuged and the solvent was removed. The crude product was washed with water and centrifuged again for 5 min. The water was decanted and the solid was dried in a vacuum oven at 50 degrees to give 3-(2′-methoxymethyl-biphenyl-4-yloxymethyl)-benzoic acid. Mass spectrum MH+=349.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07524870B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-c9601f4c2c5e44f3931ebeb5324b824b |
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| Source note | uspto-grants-2009_04 |
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