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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2418966Generated: November 2, 2026

2-Bromopyridine → HCID 14098122, compound

https://huagongshe.com/reaction/2418966

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
ReactantVeratraldehydeHCID 8419—
ReactantAmmonium HydroxideHCID 14923—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
ProductHCID 14098122HCID 14098122—

Reaction Steps

A stirred solution of 187.5 ml of 1.6 M solution of butyllithium in hexane was cooled to -40° under nitrogen and 39.5 g (0.25 M) of 2-bromopyridine in 100 ml of ether added dropwise. The mixture was stirred 15 minutes at -40° and a solution of 41.5 g (0.25 M) of 3,4-dimethoxybenzaldehyde in 200 ml of ether added. After stirring at -15° for 45 minutes, the mixture was poured into 500 g ice/100 ml conc. HCl. The separated aqueous layer was made alkaline with conc. NH4OH, extracted with methylene chloride and the dried extract concentrated. The residual oil crystallized from benzene/hexane to give 3,4-dimethoxyphenyl-2-pyridyl carbinol, mp 92°-94°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04104275
Source datasetuspto-grants-1978_08
ORD IDord-2ad4c38171d549a79ce88c8e9f0ee931
Source noteuspto-grants-1978_08