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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424354Generated: October 27, 2026

Water → (E)-2-methoxy-5-(((2,4,6-trimethoxystyryl)sulfonyl)methyl)aniline

https://huagongshe.com/reaction/424354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium DithioniteHCID 24489—
Reactant(E)-2,4,6-Trimethoxystyryl 4-Methoxy-3-Nitrobenzyl sulfoneHCID 11502726—
SolventPropan-2-one--water (1/1)HCID 18366337—
Product(E)-2-methoxy-5-(((2,4,6-trimethoxystyryl)sulfonyl)methyl)anilineHCID 11486204—

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 2-((E)-2-(4-methoxy-3-nitrobenzylsulfonyl)vinyl)-1,3,5-trimethoxybenzene (1.3 mmol) in acetone-water (10:5, 25 mL) was heated to 50° C. After 30 min, sodium hydrosulfite (Na2S2O4, 26.3 mmol) was added slowly, and the mixture was heated at reflux (50° C.) for 1 h. The heated mixture was then cooled to room temperature (25° C.) and water (25 mL) was added. A solid precipitate formed and was separated by filtration. The filtered product was washed with aqueous sodium bicarbonate. The product was distributed between water and ethyl acetate. The ethyl acetate layer was separated and dried over anhydrous sodium sulfate. The ethyl acetate was removed under reduced pressure and the crude product obtained thereby was recrystallized from 2-propanol to yield the desired (E)-5-((2,4,6-trimethoxystyrylsulfonyl)methyl)-2-methoxybenzenamine product. m.p. 148-150° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106033B2
Source datasetuspto-grants-2012_01
ORD IDord-32404a0226404360962fc43a019b7c8a
Source noteuspto-grants-2012_01