돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17625생성일: 2026년 10월 24일

2,6-Di-tert-butyl-4-methylphenol → tert-Butyl {3-[4-cyano-2-dimethylcarbamoyl-5-methyl-6-phenyl-1,3-benzoxazol-7-yl]cyclopent-2-enyl}methylcarbamate

https://huagongshe.com/ko/reaction/17625

반응식

참여 물질

역할이름HCID투입량
반응물2,6-Di-tert-butyl-4-methylphenolHCID 31404—
반응물tert-Butyl methyl-(3-tri-n-butylstannylcyclopent-2-enyl)carbamateHCID 68584969—
반응물7-bromo-4-cyano-N,N,5-trimethyl-6-phenyl-1,3-benzoxazole-2-carboxamideHCID 68585175—
촉매HCID 178418476HCID 178418476—
용매1,4-DioxaneHCID 31275—
생성물tert-Butyl {3-[4-cyano-2-dimethylcarbamoyl-5-methyl-6-phenyl-1,3-benzoxazol-7-yl]cyclopent-2-enyl}methylcarbamateHCID 8663088788%

반응 조건

온도100 °C

반응 단계

7-Bromo-4-cyano-N,N,5-trimethyl-6-phenyl-1,3-benzoxazole-2-carboxamide (I-339) (275 mg, 0.72 mmol) and tert-butyl methyl-(3-tri-n-butylstannylcyclopent-2-enyl)carbamate (I-332) (453 mg, 0.93 mol) were dissolved in 1,4-dioxane (8 ml), and at room temperature, 2,6-di-tert-butyl-paracresol (3 mg, 0.01 mmol) and then bis(triphenylphosphine)palladium(II) dichloride (50 mg, 0.07 mmol) were added. The solution was stirred under nitrogen atmosphere at 100° C. for 24 hours, then cooled to room temperature. The insoluble matter was separated by filtration with washing with ethyl acetate. The filtrate was concentrated under reduced pressure. The solvent was evaporated away, and the resulting residue was purified by middle-pressure liquid chromatography (eluent, n-hexane:ethyl acetate=2:1, v/v) to obtain the entitled compound (316 mg, 88%) as a colorless gel.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737166B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-4d95ef807d6142039a3b348d991c8850
출처 메모uspto-grants-2010_06