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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951810Generated: October 26, 2026

4-tert-Butylphenylboronic acid → HCID 178440746, compound

https://huagongshe.com/reaction/1951810

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-Butylphenylboronic acidHCID 2734320—
ReactantHCID 178477957HCID 178477957—
ProductHCID 178440746HCID 178440746—

Reaction Steps

2-(4-Bromo-benzyl)-4-(2,4-dichloro-phenyl)-1H-imidazole (3.8 g, 10 mmol) was treated as described in general procedure G using 4-tert-butylphenylboronic acid (3.6 g, 20 mmol) to give 2-(4′-tert-butyl-biphenyl-4-ylmethyl)-4-(2,4-dichloro-phenyl)-1H-imidazole, which was treated as described in general procedure R using 1,4-diiodobenzene (13.2 g, 40 mmol) to give 2-(4′-tert-butyl-biphenyl-4-ylmethyl)-4-(2,4-dichloro-phenyl)-1-(4-iodo-phenyl)-1H-imidazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404731B2
Source datasetuspto-grants-2013_03
ORD IDord-afc190ac2ba44281a585fbfe8862cd75
Source noteuspto-grants-2013_03