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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242507Generated: November 3, 2026

4-Hydroxybenzaldehyde → 4-[2-(5-Ethyl-2-pyridinyl)-2-hydroxyethoxy]benzaldehyde

https://huagongshe.com/reaction/2242507

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantSodium HydroxideHCID 14798—
ReactantN-bromobutanimideHCID 67184—
ReactantPyridine, 5-ethyl-2-vinyl-HCID 222462—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Solventtert-ButanolHCID 6386—
Product4-[2-(5-Ethyl-2-pyridinyl)-2-hydroxyethoxy]benzaldehydeHCID 1155078783%

Reaction Steps

Into a stirred mixture of 4.5 lit. tert-butanol and 13.5 lit. water was added 1.2 Kg (9.02 mole) 5-ethyl-2-vinyl-pyridine at 25° C. To this was added 1.926 Kg (10.82 mol) N-bromosuccinimide and reaction mixture was stirred for 1.5 hr. 13.5 lit. aqueous 2N NaOH solution was added to the reaction mixture and stirring was continued for further 45 min. Progress of reaction was monitored by TLC and after completion of reaction, product was extracted with 12 lit. methyl tert-butyl ether. Layers were separated, organic layer was washed with 7.2 lit. brine solution, dried (magnesium sulfate) and concentrated under reduced pressure. The residual solid obtained was added into a stirred mixture of 1.59 Kg (13 mol) 4-hydroxy benzaldehyde dissolved in 13 lit. toluene and 523 g (130 mol) NaOH dissolved in 120 lit. water. To this was added 221 g PEG 2000 and stirred for 17 hr. at 78° C. Subsequent work-up gave 2.029 Kg (83%) 4-[2-(5-ethyl-pyridin-2-yl)-2-hydroxy-ethoxy]-benzaldehyde. m.p. 81° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07671207B2
Source datasetuspto-grants-2010_03
ORD IDord-e9fb85223bef49f8a5c06cb494f0f85d
Source noteuspto-grants-2010_03