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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566939Generated: October 29, 2026

5-Allyl-2-hydroxy-3-methoxyphenylboronic acid → 6-(2-Hydroxy-3-methoxyphenyl)-6'-(5-allyl-2-hydroxy-3-methoxyphenyl)-2,2'-bipyridine

https://huagongshe.com/reaction/566939

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Allyl-2-hydroxy-3-methoxyphenylboronic acidHCID 18616953—
Reactant6-Bromo-6'-(2-hydroxy-3-methoxyphenyl)-2,2'-bipyridineHCID 135854286—
Product6-(2-Hydroxy-3-methoxyphenyl)-6'-(5-allyl-2-hydroxy-3-methoxyphenyl)-2,2'-bipyridineHCID 13552902637%

Reaction Steps

6-(2-Hydroxy-3-methoxyphenyl)-6′-(5-allyl-2-hydroxy-3-methoxyphenyl)-2,2′-bipyridine was prepared from 6-bromo-6′-(2-hydroxy-3-methoxyphenyl)-2,2′-bipyridine and 5-allyl-2-hydroxy-3-methoxyphenylboronic acid in 37% yield using method F; δH [2H6]-DMSO 13.53,(1H, s), 13.31,(1H, s), 8.35-8.20,(4H, m), 8.16,(2H, d), 7.70,(1H, s), 7.53,(1H, s), 7.09,(1H, d), 6.93,(2H, m), 6.05,(1H, m), 5.14,(1h, d), 5.06,(1H, d), 3.85,(6H, s), 3.40,(2H, d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06177419B1
Source datasetuspto-grants-2001_01
ORD IDord-b7e86ef05f7c48558df518b152dba7c5
Source noteuspto-grants-2001_01