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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597119Generated: October 27, 2026

1-(4-Morpholinophenyl)-1-phenylprop-2-yn-1-ol → 6-Morpholino-3-(4-morpholinophenyl)-3-phenyl-3h-naphtho[2,1-b]pyran

https://huagongshe.com/reaction/1597119

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Morpholinophenyl)-1-phenylprop-2-yn-1-olHCID 286741—
Reactant4-Morpholino-2-naphtholHCID 10988042—
SolventTolueneHCID 1140—
Product6-Morpholino-3-(4-morpholinophenyl)-3-phenyl-3h-naphtho[2,1-b]pyranHCID 980614873.2%

Reaction Steps

A solution of 4-morpholino-2-naphthol (1.5 g, 6.5 mmol) and 1(4-morpholinophenyl)-1-phenylprop-2-yn-1-ol (1.92 g, 6.5 mmol) in toluene (65 cm3) containing acidic alumina (Brockmann 1), (4.0 g) was refluxed for 60 minutes. The cooled solution was filtered and the alumina was washed well with EtOAc (200 cm3). Removal of the solvent from the filtrate gave an oil which solidified on standing at room temperature. Recrystallisation from EtOAc/hexane gave 6-morpholino-3(4-morpholinophenyl)-3-phenyl-3H-naphtho[2,1-b]pyran (yield=2.4 g, theoretical yield=3.3 g 73%, m.p.=187-188° C. (uncorrected), λmax in toluene=469 nm, i.e. red-orange).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06294112B1
Source datasetuspto-grants-2001_09
ORD IDord-fc326a65b57c4e238aec0b91b55f99a2
Source noteuspto-grants-2001_09