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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 426760생성일: 2026년 10월 26일

1,5-Naphthalenedisulfonic acid → (3aRS,4SR,9aSR)-3a,4,9,9a-tetrahydro-4-phenyl-benz[f]isoindoline-2-propionic acid

https://huagongshe.com/reaction/426760

반응식

참여 물질

역할이름HCID투입량
반응물1,5-Naphthalenedisulfonic acidHCID 6666—
반응물Sodium HydroxideHCID 14798—
반응물(3aRS,4SR,9aSR)-3a,4,9,9a-tetrahydro-4-phenyl-benz[f]isoindoline-2-propionic acid methyl esterHCID 70609075—
용매Hydrochloric AcidHCID 313—
생성물(3aRS,4SR,9aSR)-3a,4,9,9a-tetrahydro-4-phenyl-benz[f]isoindoline-2-propionic acidHCID 70610061—

반응 단계

10 g of (3aRS,4SR,9aSR)-3a,4,9,9a-tetrahydro-4-phenyl-benz[f]isoindoline-2-propionic acid methyl ester are heated to the boil at reflux in 50 cc of 2 N hydrochloric acid for 5 hours. The solution is then concentrated by evaporation, the residue is dissolved in water, the pH of the solution is adjusted to 1 with caustic soda solution, and 1 equivalent of 1,5-naphthalene disulphonic acid is added, whereby the bis-1,5-naphthalene-disulphonate salt form of the title compound is obtained in sticky form. The supernatant water is poured off and the resin is triturated with acetone, whereby it crystallizes. M.P. 193°-195°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04171369
출처 데이터셋uspto-grants-1979_10
ORD IDord-5565e8652efa4e418f23c6459e25ff4c
출처 메모uspto-grants-1979_10