Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261535Generated: November 2, 2026

Cesium carbonate → Ethyl 3''-tert-butyl-4'-[4-(tert-butyldimethylsilanyloxy)butoxy]-4''-pyrrolidin-4-yl[1,1';3',1'']terphenyl-4-carboxylate

https://huagongshe.com/reaction/1261535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant(4-Bromobutoxy)(tert-butyl)dimethylsilaneHCID 582370—
ReactantEthyl 3''-tert-butyl-4'-hydroxy-4''-pyrrolidin-1-yl[1,1';3',1'']terphenyl-4-carboxylateHCID 66671790—
ReactantEthyl 3''-tert-butyl-4'-[4-(tert-butyldimethylsilanyloxy)butoxy]-4''-pyrrolidin-1-yl[1,1';3',1'']terphenyl-4-carboxylateHCID 66672253—
ProductEthyl 3''-tert-butyl-4'-[4-(tert-butyldimethylsilanyloxy)butoxy]-4''-pyrrolidin-4-yl[1,1';3',1'']terphenyl-4-carboxylateHCID 7081529797%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470871B2
Source datasetuspto-grants-2013_06
ORD IDord-bb96008485004883a5904f1bb9ccab60
Source noteuspto-grants-2013_06