HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → Methyl 3'-hydroxy-2,6,2'-trimethylbiphenyl-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 3,5-dimethyl-4-(((trifluoromethyl)sulfonyl)oxy)benzoate | HCID 11849880 | — |
| Reactant | 3-Methoxymethoxy-2-methylbenzene-1-boronic acid | HCID 22606935 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 3'-hydroxy-2,6,2'-trimethylbiphenyl-4-carboxylate | HCID 22606880 | — |
Reaction Steps
In a manner similar to that of Example 11(d), by reaction of 1.5 g (7.6 mmol) of 3-methoxymethoxy-2-methylbenzene-1-boronic acid (described in Example 11(c)) with 2 g (6.4 mmol) of methyl 3,5-dimethyl-4-trifluoromethanesulphonyloxybenzoate, 7.7 mL of 2.0M potassium carbonate solution and 370 mg (0.32 mmol) of tetrakis(triphenylphosphine)palladium, followed by deprotection in methanol, the desired product is obtained in the form of a white solid (m.p.=149° C.; m=1.34 g; Y=67%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06831106B1 |
| Source dataset | uspto-grants-2004_12 |
| ORD ID | ord-e56c1a12b8c44b7283cb59879015e6dd |
| Source note | uspto-grants-2004_12 |