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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443751Generated: October 25, 2026

Salicylaldehyde → HCID 15572710, compound

https://huagongshe.com/reaction/443751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylaldehydeHCID 6998—
ReactantSodium HydroxideHCID 14798—
Reactant1,4-Dichloro-2-butene, (2E)-HCID 642197—
ReactantTetrabutylammonium HydroxideHCID 2723671—
SolventWaterHCID 962—
ProductHCID 15572710HCID 15572710—

Reaction Steps

To 2 lt of refluxing water, 3 ml of 40% aqueous tetrabutylammonium hydroxide, 250 ml of salicylaldehyde and 280 ml of trans-1,4-dichloro-2-butene are added while vigorously stirring, followed by the dropwise addition of the solution of 83 g of sodium hydroxide in 400 ml of water at such a rate that the pH of the mixture is kept between 7 and 8 (ca 25 minutes). Thereafter the mixture is refluxed for about 6 minutes until the pH is about 7, cooled to 20° and the aqueous layer is extracted with diethyl ether. The extract is combined with the organic layer, washed with 5% aqueous sodium hydroxide, dried, evaporated, the residue distilled and the fraction boiling at 141°-147°/0.7 mmHg collected, to yield the 2-(4-chloro-trans-2-butenyloxy)-benzaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04261907
Source datasetuspto-grants-1981_04
ORD IDord-c4fd0fa19a9945cd80ce9ee3fa857981
Source noteuspto-grants-1981_04