HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 233418Erstellt: 25. Oktober 2026
4-Hydroxybenzaldehyde → 4-(4-[6-Acryloyloxyhexyloxy]phenylcarbonyloxy)benzaldehyde
https://huagongshe.com/reaction/233418
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Edukt | Water | HCID 962 | — |
| Edukt | 4-((6-(Acryloyloxy)hexyl)oxy)benzoic acid | HCID 3713565 | — |
| Katalysator | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 4-(4-[6-Acryloyloxyhexyloxy]phenylcarbonyloxy)benzaldehyde | HCID 23355800 | 92,4% |
Reaktionsschritte
0.6 g of N,N'-dicyclodicyclohexylcarbodiimide is added at room temperature while stirring to a solution of 1.0 g of 4-[6-acryloyloxyhexyloxy]benzoic acid, 0.3 g of 4-hydroxybenzaldehyde and 0.04 g of 4-dimethylaminopyridine in 20 ml of dichloromethane. The reaction mixture is stirred at room temperature overnight, poured into 100 ml of water and then extracted three times with 50 ml of dichloromethane each time. The combined organic phases are washed twice with 100 ml of water each time, dried over magnesium sulphate, filtered and the filtrate is subsequently concentrated. Chromatographic purification of the residue on silica gel with hexane/ethyl acetate (vol. 1:1) and two-fold recrystallization from ethanol of the fractions which are pure according to thin-layer chromatography gives 0.9 g of 4-(4-[6-acryloyloxyhexyloxy]phenylcarbonyloxy)benzaldehyde.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05593617 |
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| Quelldatensatz | uspto-grants-1997_01 |
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| ORD ID | ord-953181295d8246269c1c0e0eba1ecf74 |
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| Quellennotiz | uspto-grants-1997_01 |
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