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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249396Generated: October 31, 2026

Water → HCID 13532505, compound

https://huagongshe.com/reaction/1249396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 20224643HCID 20224643—
Reactant6-chloropyridin-2-olHCID 178516025—
SolventAcetoneHCID 180—
ProductHCID 13532505HCID 1353250589%

Reaction Steps

31 g (0.1 mol) of 1-bromo-3-(4-chlorobenzyloxy)-methyl-2-butanone in 200 ml of acetone are heated under reflux with 14 g (0.1 mol) of potassium carbonate and 13 g (0.1 mol) of 6-chloro-2-hydroxypyridine for 6 hours. Thereafter, the reaction mixture is poured into water and extracted with methylene chloride. The organic phase is dried over sodium sulphate and concentrated. 31.5 g (89% of theory) of 3-(4-chlorobenzyloxy)-1-(6-chloropyridin-2-yloxy)-3-methyl-2-butanone are obtained as a light-coloured oil. ##STR14##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04631288
Source datasetuspto-grants-1986_12
ORD IDord-92cd8b9c5c4f45beae1e6b48ba08c942
Source noteuspto-grants-1986_12