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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223114Generated: October 26, 2026

Methyl Acrylate → Methyl 3-(2-acetyl-4-benzyloxy-6-nitrophenyl)acrylate

https://huagongshe.com/reaction/2223114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl AcrylateHCID 7294—
ReactantTri-tert-butylphosphine tetrafluoroborateHCID 2734635—
Reactantalpha-CyclohexylcyclohexanemethanamineHCID 10774245—
Reactant2-Acetyl-4-benzyloxy-6-nitrophenyl trifluoromethanesulfonateHCID 21072824—
CatalystTetrabutylammonium IodideHCID 67553—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventDiethyl EtherHCID 3283—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 3-(2-acetyl-4-benzyloxy-6-nitrophenyl)acrylateHCID 66751245—

Reaction Conditions

Temperature80 °C

Reaction Steps

100 g of molecular sieve (4 Å), tris(dibenzylideneacetone)dipalladium (5.88 g, 6.42 mmol), tri-tert-butylphosphonium-tetrafluoroborate (3.50 g, 12.06 mmol), dicyclohexylmethylamine (81.2 mL, 0.371 mol), dried tetrabutylammonium iodide (105.8 g, 0.286 mol), and methyl acrylate (32.6 mL, 0.362 mol) are added to a solution of 2-acetyl-4-benzyloxy-6-nitrophenyl trifluoromethanesulfonate (100.0 g, 0.238 mol) in dioxane (360 mL) under a nitrogen atmosphere. The reaction mixture is stirred for 2 hours at 80° C., diluted with ether (2 L) and combined with 500 g silica gel. The suspension is stirred for 10 minutes, filtered, and the silica gel is washed several times with ether (4×600 mL). The combined organic phases are washed with 1 M aqueous hydrochloric acid (300 mL), sodium bicarbonate solution, and sodium chloride solution, dried with sodium sulfate, and evaporated down. The oily crude product is recrystallized from hot ethanol (0.75 L). The precipitate is filtered off, washed with ethanol (2×50 mL) and dried at 40° C. Yield: 32.2 g (38%); mass spectroscopy: [M+H]+=356.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375104B2
Source datasetuspto-grants-2008_05
ORD IDord-53254a62c66d4eba8fba5d1064950316
Source noteuspto-grants-2008_05