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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1899756Generated: November 1, 2026

4-(Aminomethyl)cyclohexanecarboxylic acid → Coumarin

https://huagongshe.com/reaction/1899756

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Aminomethyl)cyclohexanecarboxylic acidHCID 5526—
ReactantCoumarin 314HCID 72653—
ReactantCyclopenta[c][1]benzopyran-4(1H)-one, 7-(dimethylamino)-2,3-dihydro-HCID 100527—
ReactantMethanol--water (1/1)HCID 22242641—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductCoumarinHCID 323—

Reaction Steps

To a vigorously stirred 200 mL suspension 0.282 micrometer carboxylate-modified latex (Interfacial Dynamics Corp., Portland, Oreg.; 2.75% solids in 50% v/v distilled water/methanol) is added a solution of 30 mg of Coumarin 138 (Eastman Kodak, Rochester, N.Y.) and 30 mg of Coumarin 314 (Eastman Kodak) dissolved in a homogeneous mixture of 7.5 mL of dichloromethane and 17.5 mL of absolute ethanol. The addition of the dye and purification of the product is carried out as described in EXAMPLE 3. Visual analysis of a dilute aqueous suspension of the product by fluorescence microscopy using standard AMCA excitation and emission filters shows uniformly dyed particles that are highly monodisperse. Spectral analysis of the product, exciting at 360 nm shows an emission peak centered at 410 nm and an emission peak centered at 460 nm. The integrated ratio of the 460 nm peak (from coumarin 314) to the 410 peak (from coumarin 138) is 92:8, indicating efficient transfer of emission energy from coumarin 138 to coumarin 314.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05573909
Source datasetuspto-grants-1996_11
ORD IDord-7ad6a76708284737bf19a6453ca7843c
Source noteuspto-grants-1996_11