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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807345Generated: October 31, 2026

4-(Dibutylamino)benzaldehyde → HCID 46850905, compound

https://huagongshe.com/reaction/1807345

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Dibutylamino)benzaldehydeHCID 605391—
ReactantHCID 16207064HCID 16207064—
ProductHCID 46850905HCID 46850905—

Reaction Steps

To a dry vial was added the salt 6 (708 mg, 2 mmol), 4-dibutylaminobenzaldehyde (467 mg, 2 mmol) and the vial was purged with N2. Ethanol (10 ml) was added via syringe, followed by piperidine (1 ml). Within 5 minutes the color began changing to deep red. The mixture was stirred at room temperature for 12 hours, concentrated and the salt was precipitated with dry ether. Following solvent removal, the salt was again dissolved in EtOH (8 ml) and precipitated with ether. The resulting fluorophore was filtered under a nitrogen atmosphere and dried. Yield: 1.04 g (91%). MS (dual ESI+): 204.69186 (M+H+)2+ HRMS calc. 409.3457. H-NMR (DMSO-D6): 0.92 (t, J=12 Hz, 6H); 1.38 (m, 4H); 1.48 (m, 4H); 2.24 (m, 2H); 3.22l-3.35 (m, 11 H); 3.85 (t, J=9 Hz, 4H); 4.25 (t, J=12 Hz, 2H); 6.8 (d, J=8 Hz, 2H); 6.97 (s, 2H); 7.75 (d, J=8 Hz, 2H); 8.05 (d, J=6 Hz, 2H); 8.95 (d, J=6 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357350B2
Source datasetuspto-grants-2013_01
ORD IDord-deeba0d3b9194d52a8918563e1b98c18
Source noteuspto-grants-2013_01