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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 276162생성일: 2026년 10월 24일

Benzaldehyde → Phosphine

https://huagongshe.com/ko/reaction/276162

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참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물Benzoic AcidHCID 243—
반응물TolueneHCID 1140—
반응물AnilineHCID 6115—
반응물1-HexeneHCID 11597—
반응물2-Amino-3-methylpyridineHCID 15347—
반응물PhosphineHCID 24404—
생성물PhosphineHCID 24404—
생성물HeptanophenoneHCID 74282—

반응 조건

온도130 °C

반응 단계

Under the same reaction procedure and conditions as in Example 1 (benzaldehyde 0.5 mmol, 2-amino-3-picoline 0.1 mmol, aniline 0.3 mmol, bezoic acid 0.03 mmol, 1-hexene 2.5 mmol, toluene 0.87 mmol), the mixture in a 500 ml pressure reactor was stirred at normal temperature for 2-3 minutes and then [Rh(C8H14)2Cl]2 0.01 mmol and various phosphine ligands 0.025 mmol as shown in the following table 7 were introduced into each reactor. While the reactor was stopped with a stopper, the reactants were heated at 130° C. for 1 hour with stirring. After completion of the reaction, gas chromatography was conducted to determine the yields of heptanophenone, products from various phosphine ligands. The results are given in Table 7, below.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06353139B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-e7fd9fc248924b249dac1da98ef8d5c3
출처 메모uspto-grants-2002_03