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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556280Generated: October 26, 2026

Triethylamine → 4-Formylcinnamic acid tert-butyl ester

https://huagongshe.com/reaction/556280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl acrylateHCID 15458—
Reactant4-BromobenzaldehydeHCID 70741—
ReactantSodium BicarbonateHCID 516892—
CatalystTriphenylphosphineHCID 11776—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-Formylcinnamic acid tert-butyl esterHCID 5414760470%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 4-bromo benzaldehyde (2 g, 10.8 mmol) in DMF (50 ml) and triethylamine (3.4 ml, 27 mmol) was degassed flushing N2 for 30 min. PPh3 (141 mg, 0.54 mmol), Pd(OAc)2 (48.4 mg, 0.21 mmol), NaHCO3 (1.84 g, 21.6 mmol) and tert-butyl acrylate (1.58 ml, 10.8 mmol) were added and the resulting mixture was heated to reflux for 3 h. Additional Pd(OAc)2 (24 mg) was added and the mixture was heated to 100° C. for 1 h. The solution was diluted with H2O and extracted with Et2O. The organic layer was dried over Na2SO4 and the solvent was evaporated under vacuo to give the crude product that was triturated in isopropyl ether to give 1.6 g of 3-(4-formyl-phenyl)-acrylic acid tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058273B2
Source datasetuspto-grants-2011_11
ORD IDord-4c0e5a8c3bc640fb8024f6cba150baa7
Source noteuspto-grants-2011_11