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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33379생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/33379

반응식

참여 물질

역할이름HCID투입량
반응물Methyl AcrylateHCID 7294—
반응물Tri-tert-butylphosphine tetrafluoroborateHCID 2734635—
반응물alpha-CyclohexylcyclohexanemethanamineHCID 10774245—
반응물2-Acetyl-4-benzyloxy-6-nitrophenyl trifluoromethanesulfonateHCID 21072824—
촉매Tetrabutylammonium IodideHCID 67553—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매Diethyl EtherHCID 3283—
용매1,4-DioxaneHCID 31275—
생성물Methyl 3-(2-acetyl-4-benzyloxy-6-nitrophenyl)acrylateHCID 66751245—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429583B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-75969647c2494c0a89201f948e5b0b16
출처 메모uspto-grants-2008_09