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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | N-Methyl dicyclohexylamine | HCID 24210 | — |
| Reactant | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Reactant | tert-butyl N-(1-(4-bromophenyl)ethyl)carbamate | HCID 11983730 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-[4-(1-tert-Butoxycarbonylamino-ethyl)-phenyl]-acrylic acid ethyl ester | HCID 69064356 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07504403B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-3548fe0a340042d59fd4d020a5eaab90 |
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| Source note | uspto-grants-2009_03 |
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