HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443751Generated: October 25, 2026
Salicylaldehyde → HCID 15572710, compound
https://huagongshe.com/reaction/443751
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Salicylaldehyde | HCID 6998 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,4-Dichloro-2-butene, (2E)- | HCID 642197 | — |
| Reactant | Tetrabutylammonium Hydroxide | HCID 2723671 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15572710 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04261907 |
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| Source dataset | uspto-grants-1981_04 |
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| ORD ID | ord-c4fd0fa19a9945cd80ce9ee3fa857981 |
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| Source note | uspto-grants-1981_04 |
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