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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487903Generated: October 25, 2026

3-Pyridinecarboxaldehyde → 6-Methoxy-3-(3-pyridyl)methylene-4-chromanone

https://huagongshe.com/reaction/487903

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-PyridinecarboxaldehydeHCID 10371—
ReactantPyrrolidineHCID 31268—
Reactant6-methoxy-3,4-dihydro-2H-1-benzopyran-4-oneHCID 4612168—
SolventMethanolHCID 887—
Product6-Methoxy-3-(3-pyridyl)methylene-4-chromanoneHCID 5381307957%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a 25° C. mixture of 20.0 g (0.112 mol) of 6-methoxy-4-chromanone and 18.09 g (0.169 mol) of 3-pyridinecarbaldehyde in 100 ml of methanol was added 14.1 ml (0.169 mol) of pyrrolidine. The resultant solution was allowed to stir 60 hours at 25° C., cooled to 0° C. and filtered to yield 17.07 g (57%) of the title compound, mp 127°-131° C.; MS (m/e) 267 (M+), 238, 161, 150 (100%), 135 and 107. IR (CHCl3) 1671 (C=O), 1614, 1589 and 1566 cm-1. 1H-NMR (CDCl3) delta (ppm): 3.79 (s, OCH3), 5.23 (d, J=1.5 Hz, CH2), 6.86 (d, J=8 Hz, C-8 H), 7.06 (dd, J=8, 2 Hz, C-7 H), 7.37 (d, J=1.5 Hz, vinyl H), 7.36, 7.58, 7.75, 8.52 and 8.57 (multiplets, 5 ArH). Anal. C 71.72, H 4.85, N 5 16, calcd. C 71.90 , H 4.90, N 5.24.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05298512
Source datasetuspto-grants-1994_03
ORD IDord-8ed68baaff564c0d9de4b5621149b546
Source noteuspto-grants-1994_03