HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cesium carbonate → Ethyl 3''-tert-butyl-4'-[4-(tert-butyldimethylsilanyloxy)butoxy]-4''-pyrrolidin-4-yl[1,1';3',1'']terphenyl-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | (4-Bromobutoxy)(tert-butyl)dimethylsilane | HCID 582370 | — |
| Reactant | Ethyl 3''-tert-butyl-4'-hydroxy-4''-pyrrolidin-1-yl[1,1';3',1'']terphenyl-4-carboxylate | HCID 66671790 | — |
| Reactant | Ethyl 3''-tert-butyl-4'-[4-(tert-butyldimethylsilanyloxy)butoxy]-4''-pyrrolidin-1-yl[1,1';3',1'']terphenyl-4-carboxylate | HCID 66672253 | — |
| Product | Ethyl 3''-tert-butyl-4'-[4-(tert-butyldimethylsilanyloxy)butoxy]-4''-pyrrolidin-4-yl[1,1';3',1'']terphenyl-4-carboxylate | HCID 70815297 | 97% |
Reaction Steps
In a manner similar to that of Example 2a, by reacting 123 mg of ethyl 3″-tert-butyl-4′-hydroxy-4″-pyrrolidin-1-yl[1,1′;3′,1″]terphenyl-4-carboxylate (0.27 mmol) with 110 mg (0.34 mmol) of caesium carbonate and 80 μL of 1-bromo-4-(tert-butyldimethylsilanyloxy)butane (0.30 mmol), 170 mg of ethyl 3″-tert-butyl-4′-[4-(tert-butyldimethylsilanyloxy)butoxy]-4″-pyrrolidin-1-yl[1,1′;3′,1″]terphenyl-4-carboxylate are obtained (yield=97%) in the form of an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08470871B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-bb96008485004883a5904f1bb9ccab60 |
| Source note | uspto-grants-2013_06 |