Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1183216Generated: November 2, 2026

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

https://huagongshe.com/reaction/1183216

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 (13 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 numberUS08664272B2
Source datasetuspto-grants-2014_03
ORD IDord-47beeef67dab498ebd8f3c0fe05ecb3a
Source noteuspto-grants-2014_03