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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785442Generated: October 31, 2026

Ethyl Acrylate → 3-[4-(1-tert-Butoxycarbonylamino-ethyl)-phenyl]-acrylic acid ethyl ester

https://huagongshe.com/reaction/1785442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcrylateHCID 8821—
ReactantN-Methyl dicyclohexylamineHCID 24210—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
Reactanttert-butyl N-(1-(4-bromophenyl)ethyl)carbamateHCID 11983730—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product3-[4-(1-tert-Butoxycarbonylamino-ethyl)-phenyl]-acrylic acid ethyl esterHCID 69064356—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of [1-(4-bromo-phenyl)-ethyl]-carbamic acid tert-butyl ester (3.0 g, 10 mmol), tris(dibenzylideneacetone)dipalladium (0.55 g, 0.6 mmol), and N -methyldicyclohexylamine (2.1 mL, 10 mmol) was purged nitrogen followed by the addition of 1,4-dioxane (20 mL) and tri-tert-butylphospine (0.24 g, 1.2 mmol). The mixture was again purged with nitrogen and the ethyl acrylate (2.16 mL, 20 mmol) was added. The mixture was heated to 80° C. for 30 min, poured into water (100 mL) and extracted with ethyl acetate (150 mL). The organic layer was separated, washed again with water, dried over magnesium sulfate, concentrated and chromatographed on silica gel using 2:1 hexanes/ethyl acetate to afford a light-brown oil. M+1=320.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504403B2
Source datasetuspto-grants-2009_03
ORD IDord-3548fe0a340042d59fd4d020a5eaab90
Source noteuspto-grants-2009_03