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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1739759생성일: 2026년 10월 27일

Acrylonitrile → Benzyltriethylammonium hydroxide

https://huagongshe.com/reaction/1739759

반응식

참여 물질

역할이름HCID투입량
반응물AcrylonitrileHCID 7855—
반응물1,4-DioxaneHCID 31275—
반응물2-Nitropyridin-3-amineHCID 83281—
반응물3-Amino-4-nitropyridineHCID 586943—
생성물Benzyltriethylammonium hydroxideHCID 74601—

반응 단계

An aminonitropyridine derivative II, such as 3-amino4-nitropyridine, may be treated with a mixture of acrylonitrile and a suitable base such as Triton B (N-benzyltriethylammonium hydroxide) in an appropriate solvent such as dioxane at room temperature for 1-4 days to give the illustrated nitrile derivative III. Treatment of derivative III with a suitable reduction catalyst such as Pd/C in an appropriate solvent such as ethyl acetate under hydrogen atmosphere of about 50-60 psig for about 3-12 h gives the amino derivative IV. This derivative may be heated with ethyl ethoxycarbonylacetimidate hydrochloride in a suitable solvent such as EtOH for about 4-24 h to give the the ester V. Treatment of derivative V with an anhydrous acid such as HCl(g) in an appropriate solvent such as EtOH at reflux for 4-24 h gives the diester VI. This diester may be treated with a suitable base such as sodium ethoxide in an appropriate solvent such as EtOH for about 12-24 h at room temperature followed by treatment with ethanolic HCl to give the derivative

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05968946
출처 데이터셋uspto-grants-1999_10
ORD IDord-67fbae588a7346c59b4d397f6ee914c0
출처 메모uspto-grants-1999_10