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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158166Generated: November 1, 2026

Ethyl 3'-bromo-4'-[3-(tert-butyldimethylsilanyloxy)propoxy]biphenyl-4-carboxylate → Ethyl 4'-[3-(tert-butyldimethylsilanyloxy)propoxy]-4''-diethylamino-3''-methyl[1,1';3',1'']terphenyl-4-carboxylate

https://huagongshe.com/reaction/1158166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3'-bromo-4'-[3-(tert-butyldimethylsilanyloxy)propoxy]biphenyl-4-carboxylateHCID 66671827—
Reactant4-Diethylamino-3-methylphenylboronic acidHCID 66672056—
CatalystHCID 178418397HCID 178418397—
ProductEthyl 4'-[3-(tert-butyldimethylsilanyloxy)propoxy]-4''-diethylamino-3''-methyl[1,1';3',1'']terphenyl-4-carboxylateHCID 6667222595.5%

Reaction Steps

In a manner similar to that of Example 1d, by reacting 1 g (2 mmol) of ethyl 3′-bromo-4′-[3-(tert-butyldimethylsilanyloxy)propoxy]biphenyl-4-carboxylate (obtained in Example 6b) with 630 mg of 4-diethylamino-3-methylphenylboronic acid (3 mmol) in the presence of tetrakis(triphenylphosphine)palladium, 1.1 g of ethyl 4′-[3-(tert-butyldimethylsilanyloxy)propoxy]-4″-diethylamino-3″-methyl[1,1′;3′,1″]terphenyl-4-carboxylate (yield=95%) are obtained in the form of a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807708B2
Source datasetuspto-grants-2010_10
ORD IDord-d3620f42482d4227a2d27f32349e69ee
Source noteuspto-grants-2010_10