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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64417Generated: October 25, 2026

Toluene → ethyl (2E)-3-(2-{[(tert-butoxycarbonyl)amino]methyl}phenyl)acrylate

https://huagongshe.com/reaction/64417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Bromo-N-(tert-butoxycarbonyl)benzylamineHCID 7018300—
Reactant(E)-Ethyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)acrylateHCID 23553751—
Catalystpalladium(II) acetateHCID 167845—
SolventDiethyl EtherHCID 3283—
Productethyl (2E)-3-(2-{[(tert-butoxycarbonyl)amino]methyl}phenyl)acrylateHCID 8671342738.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 1 g of tert-butyl (2-bromobenzyl)carbamate, 1.12 g of ethyl (2E)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)acrylate, 16 mg of palladium acetate, 72 mg of dicyclohexyl(2′,6′-dimethoxybiophenyl-2-yl)phosphine, 1.5 g of potassium phosphate, and 20 mL of toluene was stirred at 100° C. for 5 days. To the reaction mixture was added ether, followed by filtration through silica gel. The filtrate was concentrated under reduced pressure and the obtained residue was purified by silica gel column chromatography to obtain 412 mg of ethyl (2E)-3-(2-{[(tert-butoxycarbonyl)amino]methyl}phenyl)acrylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447090B2
Source datasetuspto-grants-2016_09
ORD IDord-52bab543b59d45a5b32662ed568d4b3a
Source noteuspto-grants-2016_09