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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-bromopropionateHCID 95576—
ReactantSodium AcetateHCID 517045—
Reactant(E)-2-methoxy-5-(((2,4,6-trimethoxystyryl)sulfonyl)methyl)anilineHCID 11486204—
SolventMethanolHCID 887—
Productmethyl(E)-2-(5-((2,4,6-trimethoxystyrylsulfonyl)methyl)-2-methoxyphenylamino)propanoateHCID 54579438—

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106033B2
Source datasetuspto-grants-2012_01
ORD IDord-41c1bd4802a94b8a8b46f77e775630f2
Source noteuspto-grants-2012_01