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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261532Generated: November 2, 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/1261532

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 numberUS08470871B2
Source datasetuspto-grants-2013_06
ORD IDord-cb2c3473364c4b2583a952082497f605
Source noteuspto-grants-2013_06