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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1105502Generated: October 29, 2026

Hydrochloric Acid → 2-(4-Chloro-trans-2-butenyloxy)-benzaldehyde

https://huagongshe.com/reaction/1105502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSalicylaldehydeHCID 6998—
Reactant1,4-Dichloro-2-butene, (2E)-HCID 642197—
ReactantSodium MethoxideHCID 10942334—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product2-(4-Chloro-trans-2-butenyloxy)-benzaldehydeHCID 15572710—

Reaction Steps

To 130 lt of ethanol, 12.1 kg of sodium methoxide are added while cooling and stirring, followed by 26.5 kg of salicylaldehyde at 30°. Thereupon 33.3 kg of trans-1,4-dichloro-2-butene are added and the mixture heated to 68° for 4 hours. It is combined with 156 lt of toluene, 187 lt of water and 9.4 kg of 36% hydrochloric acid while keeping the temperature at about 30°. The precipitate formed is filtered off and washed with 16 lt of toluene. The filtrate is separated, the organic layer washed 3 times with 27 lt of water, evaporated, the residue distilled and the fraction boiling at 170°/0.2 mmHg collected, to yield the 2-(4-chloro-trans-2-butenyloxy)-benzaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04309349
Source datasetuspto-grants-1982_01
ORD IDord-c82aeb63d1214da19af69ee3431e9888
Source noteuspto-grants-1982_01