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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 65394생성일: 2026년 10월 24일

Sulfuric Acid → 4-octyloxy-4'-((S)-3-methyl-pentanoyl)biphenyl

https://huagongshe.com/ko/reaction/65394

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물TolueneHCID 1140—
반응물1-Bromo-2-methylbutaneHCID 25254—
반응물[1,1'-Biphenyl]-4-carbonitrile, 4'-(octyloxy)-HCID 104173—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물4-octyloxy-4'-((S)-3-methyl-pentanoyl)biphenylHCID 13685070—

반응 단계

Sliced Mg (12.4 g, 0.510 mol) and dry ether (50 ml) were placed in a three-neck flask in a dry nitrogen atmosphere and agitated, and to the mixture was dropwise added a solution obtained by dissolving (+)-2-methylbutyl bromide (prepared from (-)-2-methyl-1-butanol and phosphorus bromide) in dry ether (1 l), so as to keep the temperature of the system at 25° C. or lower. After completion of the dropwise addition, the mixture was allowed to stand at room temperature for 30 minutes, followed by dropwise adding a solution obtained by dissolving a commercially available product, 4-octyloxy-4'-cyanobiphenyl (IV) (129 g, 0.42 mol) in dry ether (1 l) so as to keep the temperature of the system at 10° C. or lower, thereafter refluxing for 4 hours, cooling pouring the reaction liquid in water (600 ml), further adding diluted sulfuric acid (conc. sulfuric acid 40 ml +water 80 ml, adding toluene (500 ml), transferring the mixture into a separating funnel, water-washing till the washing liquid became neutral, distilling off the solvent, distilling the residue under reduced pressure, collecting a fraction of bp 245°~255° C./4 mmHg and recrystalling from acetone (30 ml) to obtain 4-octyloxy-4'-((S)-3-methyl-pentanoyl)biphenyl (IIIa1) (24.6 g), which was a smectic liquid crystal exhibiting SC* phase and SA phase, and its phase transition points were as follows as shown in Table 2, column of Example 23:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04614609
출처 데이터셋uspto-grants-1986_09
ORD IDord-e153a6315c0a4414914c455b97d150b8
출처 메모uspto-grants-1986_09