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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74257생성일: 2026년 10월 25일

2-(4-Neopentylamino-3-nitrophenyl)benzoxazole → 2-(2-Neopentylaminoanilin-5-yl)benzoxazole

https://huagongshe.com/reaction/74257

반응식

참여 물질

역할이름HCID투입량
반응물2-(4-Neopentylamino-3-nitrophenyl)benzoxazoleHCID 67499014—
반응물HCID 178418361HCID 178418361—
촉매HCID 178418390HCID 178418390—
용매TetrahydrofuranHCID 8028—
생성물2-(2-Neopentylaminoanilin-5-yl)benzoxazoleHCID 6749786689.2%

반응 단계

To a tetrahydrofuran solution (5 mL) of 2-(4-neopentylamino-3-nitrophenyl)benzoxazole (see Working Example 81-1) (242 mg, 0.744 mmol) was added 10% palladium-carbon (40 mg), a hydrogen atmosphere was substituted in the flask, and this was stirred at room temperature for 15 hours. After the reaction was complete, this was filtered through Celite and the filtrate was concentrated. The residue obtained was purified by silica gel column chromatography to yield the title compound (196 mg, 89% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829035B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-11f03d1e0fb8423a8aaa20d19de03e28
출처 메모uspto-grants-2014_09