HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424355Generated: October 28, 2026
Methyl 2-bromopropionate → methyl(E)-2-(5-((2,4,6-trimethoxystyrylsulfonyl)methyl)-2-methoxyphenylamino)propanoate
https://huagongshe.com/reaction/424355
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 2-bromopropionate | HCID 95576 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | (E)-2-methoxy-5-(((2,4,6-trimethoxystyryl)sulfonyl)methyl)aniline | HCID 11486204 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | methyl(E)-2-(5-((2,4,6-trimethoxystyrylsulfonyl)methyl)-2-methoxyphenylamino)propanoate | HCID 54579438 | — |
Reaction Steps
Sodium acetate (0.4 mol) was dissolved in methanol (200 mL). Methyl-2-bromopropionate (40 mmol) was added and the resulting mixture was heated at reflux for 10 min. The heated mixture was cooled to room temperature (25° C.), and (E)-5-((2,4,6-trimethoxystyrylsulfonyl)methyl)-2-methoxybenzenamine (0.1 mol) was added. The resulting mixture was heated at reflux for 1 h. The hot reaction mixture was allowed to cool to room temperature (25° C.), and then poured into ice water (500 mL). A solid precipitate formed. The precipitate was separated by filtration and recrystallized from ethanol to provide the desired methyl(E)-2-(5-((2,4,6-trimethoxystyrylsulfonyl)methyl)-2-methoxyphenylamino)propanoate.
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-41c1bd4802a94b8a8b46f77e775630f2 |
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| Source note | uspto-grants-2012_01 |
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