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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158169Generated: November 2, 2026

Potassium Carbonate → Ethyl 3''-tert-butyl-4-hydroxy-4''-pyrrolidin-1-yl[1,1';3',1'']terphenyl-4-carboxylate

https://huagongshe.com/reaction/1158169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 3'-bromo-4'-hydroxybiphenyl-4-carboxylateHCID 16657517—
ReactantEthyl 3''-tert-butyl-4'-hydroxy-4''-pyrrolidin-1-yl[1,1';3',1'']terphenyl-4-carboxylateHCID 66671790—
Reactant(3-(Tert-butyl)-4-(pyrrolidin-1-yl)phenyl)boronic acidHCID 66672251—
CatalystHCID 178418397HCID 178418397—
ProductEthyl 3''-tert-butyl-4-hydroxy-4''-pyrrolidin-1-yl[1,1';3',1'']terphenyl-4-carboxylateHCID 8661789863%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807708B2
Source datasetuspto-grants-2010_10
ORD IDord-24edd09aec4247748ee84274ead5f41f
Source noteuspto-grants-2010_10