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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199493Generated: October 31, 2026

Hydrochloric Acid → 5-[(E)-2-(3,5-Dimethoxyphenyl)ethenyl]-2-methoxyphenol

https://huagongshe.com/reaction/2199493

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium MethoxideHCID 10942334—
ReactantPhenol, 5-[2-(3,5-dimethoxyphenyl)ethenyl]-2-methoxy-, acetate, (E)-HCID 13888665—
SolventMethanolHCID 887—
Product5-[(E)-2-(3,5-Dimethoxyphenyl)ethenyl]-2-methoxyphenolHCID 538508686.1%

Reaction Steps

Dissolve compound 21c (5.0 g, 0.015 mol) in anhydrous methanol (50 ml), add in sodium methoxide (1.41 g, 0.024 mol), reflux to react for 3h, after completion of the reaction, pour the reaction solution into ice water, adjust pH to less than 2 with dilute hydrochloric acid, extract three times with ethyl acetate, pool the organic layer, dry the solution over anhydrous magnesium sulfate. Filter, and evaporate the solvent in the solution, redissolve the residue with petroleum ether/ethyl acetate, recrystallize to obtained a white solid (3.70 g, 85%). 1H NMR (400 MHz, DMSO-d6): 3.75 (s, 3H), 3.81 (s, 6H), 6.24 (s, 1H), 6.86 (s, 2H), 6.93 (d, J=16.0 Hz, 1H), 7.01 (d, J=16.0 Hz, 1H), 7.08 (d, J=7.6 Hz, 1H), 7.13 (d, J=7.6 Hz, 1H), 7.15 (s, 1H), 9.89 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359298B2
Source datasetuspto-grants-2016_06
ORD IDord-a06bcce6a68047aeb0a92d78948acda9
Source noteuspto-grants-2016_06