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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095273Generated: October 25, 2026

3,4,5-Trimethoxyphenol → 2'-Hydroxy-4',5',6'-trimethoxy-4-nitrochalcone

https://huagongshe.com/reaction/1095273

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4,5-TrimethoxyphenolHCID 69505—
Reactant3-(4-nitrophenyl)prop-2-enoyl ChlorideHCID 319463—
Product2'-Hydroxy-4',5',6'-trimethoxy-4-nitrochalconeHCID 7276706922%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 3,4,5-trimethoxyphenol (1.85 g, 10 mmol) and 4-nitrocinnamoyl chloride (2.11 g, 10 mmol) was dissolved in BF3-Et2O complex (10 ml) and heated to 80° C. for 10 min, and then quenched with excess of water. The aqueous layer was extracted with dichloromethane. The combined organic layer was concentrated and the residue was purified by column chromatography on silica gel (CH2Cl2:EtOAc:Hexane=1:1:3) gave 7a (0.79 g, 22%) and 7b (1.54 g, 43%). 1H NMR (400 MHz, CDCl3) μ 3.81 (s, 3H), 3.90 (s, 3H), 3.91 (s, 3H), 6.29 (s, 1H), 7.74 (d, J=8.8 Hz, 2H), 7.76 (d, J=16.0 Hz, 1H), 8.01 (d, J=16.0 Hz, 1H), 8.26 (d, J=8.8 Hz, 2H), 13.44 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138165B2
Source datasetuspto-grants-2012_03
ORD IDord-4049c48a3e50449dade86f120b203cfc
Source noteuspto-grants-2012_03