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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74466생성일: 2026년 10월 24일

2-Methyl-2-butanol → N-benzhydrylidene-N'-(3,5-di-tert-butyl-phenyl)-hydrazine

https://huagongshe.com/ko/reaction/74466

반응식

참여 물질

역할이름HCID투입량
반응물2-Methyl-2-butanolHCID 6405—
반응물DiphenylmethylidenehydrazineHCID 79304—
반응물1-Bromo-3,5-di-tert-butylbenzeneHCID 620136—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
촉매palladium(II) acetateHCID 167845—
용매1,2-DimethoxyethaneHCID 8071—
생성물N-benzhydrylidene-N'-(3,5-di-tert-butyl-phenyl)-hydrazineHCID 86669219—

반응 조건

온도60 °C

반응 단계

Palladium acetate (8.4 mg, 0.037 mmol) and 2-dicyclohexylphosphino-2′,4′,6′-tri-i-propyl-1,1′-biphenyl (X-PHOS) (35.6 mg, 0.074 mmol) were dissolved in tert-amyl alcohol (10 μl, 0.093 mmol) and anhydrous ethylene glycol dimethyl ether (0.25 ml). The mixture was heated and stirred at 60° C. for five minutes under a nitrogen atmosphere to prepare a catalyst. In a separate reaction container under a nitrogen atmosphere, 1-bromo-3,5-di-t-butyl benzene (501 mg, 1.9 mmol), lithium bis(trimethylsilyl) amide (475 mg, 2.8 mmol), and benzophenone hydrazone (401 mg, 2.0 mmol) were dissolved in anhydrous ethylene glycol dimethyl ether (2.5 ml). Then, a solution containing the prepared catalyst was added thereto. After deaeration, this was heated and stirred at 90° C. for two hours under a nitrogen atmosphere. The reaction mixture was cooled to room temperature, and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate=100/5). Thus, N-benzhydrylidene-N′-(3,5-di-tert-butyl-phenyl)-hydrazine was obtained as a yellow amorphous material (699 mg, 97.7%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829199B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-bf913cf0e23b45e882f43ade3f130e66
출처 메모uspto-grants-2014_09