HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171882Generated: October 26, 2026
Methanol → Ethyl (4'-methylbiphenyl-2-yl)acetate
https://huagongshe.com/reaction/1171882
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Tolylboronic acid | HCID 79799 | — |
| Reactant | Ethyl 2-(2-bromophenyl)acetate | HCID 2780092 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl (4'-methylbiphenyl-2-yl)acetate | HCID 86245029 | — |
Reaction Steps
To a mixture composed of 243.1 mg (1 mmol) of ethyl 2-(2-bromophenyl)acetate, 3.7 ml of toluene, 57.8 mg (0.05 mmol) of tetrakis(triphenylphosphine)palladium and 127.2 mg (1.2 mmol) of anhydrous sodium carbonate are added 169.9 mg (1.25 mmol) of 4-methylphenylboronic acid, followed by addition of 2.21 ml (0.055 mmol) of methanol. The reaction medium is heated at 85° C. for 16 hours with stirring. After cooling, 10 ml of water and 8 ml of ethyl acetate are added with stirring, and the mixture is then filtered through a fluted filter paper. The organic phase is recovered and the aqueous phase is extracted again with ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07829721B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-59a9caae248d43a8abbb9a25d5b4f2aa |
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| Source note | uspto-grants-2010_11 |
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