HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354120Generated: November 3, 2026
Malonaldehyde bis(phenylimine) monohydrochloride → HCID 86614813, compound
https://huagongshe.com/reaction/2354120
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Malonaldehyde bis(phenylimine) monohydrochloride | HCID 12213307 | — |
| Reactant | HCID 86614810 | HCID 86614810 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 86614813 | HCID 86614813 | — |
Reaction Steps
1-Ethyl-2,3-dimethyl-3-(4-sulphobutyl)-3H-indolium-5-sulphonate, crude (1.1 g), malonaldehyde bis(phenylimine) HCl (0.5 g) and acetic acid (20 ml) were heated under nitrogen at 130° C. for 8 hrs to give a dark orange-red solution. The solvent was then evaporated under vacuum; the residue was partitioned in a water/dichloromethane/methanol mixture. UV/Vis is analysis (ethanol) confirmed the presence of the product in the upper, aqueous layer (λmax=524 nm) while the malonaldehyde starting material was present only in the lower, organic layer (λmax=384 nm). The aqueous layer was evaporated under vacuum and purified by HPLC (water/0.1% TFA and acetonitrile/0.1% TFA eluants). Fractions containing the product were pooled and evaporated, with final drying under high vacuum over phosphorus pentoxide to give the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07750163B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-1372a3dc9b9e40c59837da5d09009386 |
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| Source note | uspto-grants-2010_07 |
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