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HRID 426760作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物1,5-Naphthalenedisulfonic acidHCID 6666—
反応物Sodium HydroxideHCID 14798—
反応物(3aRS,4SR,9aSR)-3a,4,9,9a-tetrahydro-4-phenyl-benz[f]isoindoline-2-propionic acid methyl esterHCID 70609075—
溶媒Hydrochloric AcidHCID 313—
生成物(3aRS,4SR,9aSR)-3a,4,9,9a-tetrahydro-4-phenyl-benz[f]isoindoline-2-propionic acidHCID 70610061—

反応手順

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°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04171369
出典データセットuspto-grants-1979_10
ORD IDord-5565e8652efa4e418f23c6459e25ff4c
出典メモuspto-grants-1979_10