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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | (E)-2,4,6-Trimethoxystyryl 4-Methoxy-3-Nitrobenzyl sulfone | HCID 11502726 | — |
| Solvent | Propan-2-one--water (1/1) | HCID 18366337 | — |
| Product | (E)-2-methoxy-5-(((2,4,6-trimethoxystyryl)sulfonyl)methyl)aniline | HCID 11486204 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106033B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-32404a0226404360962fc43a019b7c8a |
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| Source note | uspto-grants-2012_01 |
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