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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17616생성일: 2026년 10월 24일

Tributylphenyltin → 2-Cyclopropyl-7-methoxy-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrile

https://huagongshe.com/ko/reaction/17616

반응식

참여 물질

역할이름HCID투입량
반응물TributylphenyltinHCID 607632—
반응물2,6-Di-t-butylcresolHCID 66637192—
반응물6-Bromo-2-cyclopropyl-7-methoxy-5-methyl-1,3-benzoxazole-4-carbonitrileHCID 68584745—
촉매HCID 178418476HCID 178418476—
용매1,4-DioxaneHCID 31275—
생성물2-Cyclopropyl-7-methoxy-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrileHCID 6858485698%

반응 조건

온도100 °C

반응 단계

Under argon atmosphere, bis(triphenylphosphine)palladium(II) dichloride (777 mg, 1.11 mmol) was added to a 1,4-dioxane (110 ml) solution of 6-bromo-2-cyclopropyl-7-methoxy-5-methyl-1,3-benzoxazole-4-carbonitrile (I-83) (3.40 g, 11.1 mmol), tributylphenyltin (5.28 g, 14.4 mmol) and 2,6-di-tert-butylcresol (488 mg, 2.21 mmol), followed by stirring in an oil bath at 100° C. for 15 hours. The reaction liquid was concentrated under reduced pressure, the residue was dissolved in ethyl acetate, and washed with water and saturated brine. After drying over anhydrous sodium sulfate, the insoluble matter was separated by filtration, and the residue obtained by concentration was washed with diethyl ether to obtain the entitled compound (3.30 g, 98%) as a pale gray solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737166B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-68507d3cc36e415e80c5a36e8ee390ba
출처 메모uspto-grants-2010_06