HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → Ethyl 3''-tert-butyl-4-hydroxy-4''-pyrrolidin-1-yl[1,1';3',1'']terphenyl-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 3'-bromo-4'-hydroxybiphenyl-4-carboxylate | HCID 16657517 | — |
| Reactant | Ethyl 3''-tert-butyl-4'-hydroxy-4''-pyrrolidin-1-yl[1,1';3',1'']terphenyl-4-carboxylate | HCID 66671790 | — |
| Reactant | (3-(Tert-butyl)-4-(pyrrolidin-1-yl)phenyl)boronic acid | HCID 66672251 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | Ethyl 3''-tert-butyl-4-hydroxy-4''-pyrrolidin-1-yl[1,1';3',1'']terphenyl-4-carboxylate | HCID 86617898 | 63% |
Reaction Steps
In a manner similar to that of Example 1d, by reacting 1 g of ethyl 3′-bromo-4′-hydroxy-biphenyl-4-carboxylate (3 mmol) with 1.2 g of 3-tert-butyl-4-pyrrolidinophenylboronic acid (4.5 mmol) in the presence of 5 mL of 2M potassium carbonate (10 mmol) and 360 mg of tetrakis(triphenylphosphine)palladium (Pd(PPh3)4), 900 mg of ethyl 3″-tert-butyl-4′-hydroxy-4″-pyrrolidin-1-yl[1,1′;3′,1″]terphenyl-4-carboxylate are obtained (yield=63%) in the form of a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07807708B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-24edd09aec4247748ee84274ead5f41f |
| Source note | uspto-grants-2010_10 |