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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 376515생성일: 2026년 10월 25일

Tetrafluorophthalonitrile → 2-Phenylpropionitrile

https://huagongshe.com/reaction/376515

반응식

참여 물질

역할이름HCID투입량
반응물TetrafluorophthalonitrileHCID 74600—
반응물TetrafluoroisophthalonitrileHCID 608182—
반응물2,3,4,6-TetrafluorobenzonitrileHCID 22287549—
생성물2-PhenylpropionitrileHCID 15761—

반응 단계

By a method similar to Example 11, a reaction was carried out using 2,4,5,6-tetrafluoroisophthalonitrile, instead of 3,4,5,6-tetrafluorophthalonitrile. After 5 hours, the reaction solution was analyzed by gas chromatography, whereupon the conversion of 2,4,5,6-tetrafluoroisophthalonitrile was found to be 36% and the yield of 2,3,4,6-tetrafluorobenzonitrile (based on 2,4,5,6-tetrafluoroisophthalonitrile) was 20%. At the same time, 1.1 mmol of α-methylbenzylcyanide was produced. This corresponded to 0.35 times molar amount relative to the production of 2,3,4,6-tetrafluorobenzonitrile.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06020517
출처 데이터셋uspto-grants-2000_02
ORD IDord-41e1ed2ba8da46c882cfa7d1e54ed6d9
출처 메모uspto-grants-2000_02