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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817685Generated: October 29, 2026

Piperonal → 209158-91-8

https://huagongshe.com/reaction/1817685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperonalHCID 8438—
Reactant3',4',5'-TrimethoxyacetophenoneHCID 14345—
ReactantSodium HydroxideHCID 14798—
SolventMethanolHCID 887—
Product209158-91-8HCID 10291089—

Reaction Steps

To a stirred solution of piperonal (1.13 g, 7.5 mmol) and 3,4,5-trimethoxyacetophenone (1.58 g, 7.5 mmol) in methanol (15 ml) was added aqueous NaOH (6 ml, 50% w/v) and the mixture stirred for 18 h. The resultant solid was collected by filtration and recrystallised from methanol (100 ml) as pale yellow crystals (1.98 g, 77%): mp 135° C.; 1H NMR δ (CDCl3) 3.92 (3H, s, OCH3), 3.93 (6H, s, OCH3), 6.01 (2H, s, CH2), 6.83 (1H, d, J=8.0 Hz, H-5), 7.11 (1H, dd, J=1.6, 8.0 Hz, H-6), 7.15 (1H, d, J=1.6 Hz, H-2), 7.25 (2H, s, H-2′,6′), 7.30 (1H, d, J=15.5 Hz, CH), 7.72 (1H, d, J=15.5 Hz, CHCO); 13C NMR 56.42, 60.99, 101.69, 106.06, 106.68, 108.72, 119.77, 125.26, 133.72, 142.43, 144.60, 148.44, 149.96, 153.17, 189.07; MS (rel intensity) m/z 343 ([M+H]+, 100%); Anal. Calcd (C19H18O6): C, 66.66; H, 5.30. Found C, 66.43; H, 5.45.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598294B2
Source datasetuspto-grants-2009_10
ORD IDord-16fe2199e4e4480d9887730efdeb710d
Source noteuspto-grants-2009_10