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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 35797생성일: 2026년 10월 24일

6-Aminohexanoic Acid → 6-(cis-1,2,3,6-Tetrahydrophthalimido)hexanoic acid

https://huagongshe.com/ko/reaction/35797

반응식

참여 물질

역할이름HCID투입량
반응물6-Aminohexanoic AcidHCID 564—
반응물Tetrahydrophthalic anhydride, cis-HCID 98495—
용매Acetic AcidHCID 176—
생성물6-(cis-1,2,3,6-Tetrahydrophthalimido)hexanoic acidHCID 1551668—

반응 조건

온도4 °C

반응 단계

31 g (0.2 mole) of cis-1,2,3,6-tetrahydrophthalic anhydride and 26.2 g (0.2 mole) of 6-aminohexanoic acid are dissolved in 400 ml. of acetic acid and warmed 3 hours on a steam bath. The cooled solution is concentrated to remove most of the acetic acid and the residue taken up in 200 ml. of methylene chloride. The solution is washed twice with water and dried over sodium sulfate. The solvent is removed and the residue taken up in 500 ml toluene. Para-toluenesulfonic acid (1 g) is added to the solution, followed by reflux for 10 hrs. with a Dean-Stark water trap. The solution is cooled and concentrated to about 50 ml and diluted with 50 ml of hexane. The mixture is shaken for a few minutes until the oil crystallizes then cooled at 4° C. for several hours, filtered and dried at 50° C. The light yellow crystals (32 g) are taken up in chloroform and filtered to remove any precipitate. The solution is diluted with hexane near the cloud point, cooled until a crystalline mass accumulates, filtered and dried to yield white crystals, m.p. 85°-87° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05411869
출처 데이터셋uspto-grants-1995_05
ORD IDord-8ae8e440dc58469e85ec63cb2158cff9
출처 메모uspto-grants-1995_05