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HRID 33379作成日:2026年10月25日

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

https://huagongshe.com/reaction/33379

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl AcrylateHCID 7294—
反応物Tri-tert-butylphosphine tetrafluoroborateHCID 2734635—
反応物alpha-CyclohexylcyclohexanemethanamineHCID 10774245—
反応物2-Acetyl-4-benzyloxy-6-nitrophenyl trifluoromethanesulfonateHCID 21072824—
触媒Tetrabutylammonium IodideHCID 67553—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒Diethyl EtherHCID 3283—
溶媒1,4-DioxaneHCID 31275—
生成物Methyl 3-(2-acetyl-4-benzyloxy-6-nitrophenyl)acrylateHCID 66751245—

反応手順

5.88 g (6.42 mmol) tris-(dibenzylideneacetone)-dipalladium, 3.50 g (12.01 mmol) tri-tert-butylphosphonium tetrafluoroborate, 81.2 mL (371 mmol) dicyclohexylmethylamine, 105.8 g (286 mmol) tetrabutylammonium iodide and 32.6 mL (362 mmol) methylacrylate are added to a solution of 100 g (238 mmol) 2-acetyl-4-benzyloxy-6-nitro-phenyl trifluoromethanesulphonate in 360 mL dioxane. The reaction mixture is stirred for 2 hours at 80° C. under a nitrogen atmosphere in the presence of 100 g molecular sieve 4A and then combined with 2 L diethyl ether and 500 g silica gel. After 10 minutes the silica gel is suction filtered, while washing repeatedly with diethyl ether. The combined organic phases are washed successively with 1 N hydrochloric acid, sodium carbonate solution and sodium chloride solution. The solvent is distilled off, the residue is crystallised from ethanol and the solid is filtered off and washed with ethanol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07429583B2
出典データセットuspto-grants-2008_09
ORD IDord-75969647c2494c0a89201f948e5b0b16
出典メモuspto-grants-2008_09