Water → Bis(tropan-3-yl) succinate

HRID 650715

Reaktionsgleichung

Reaktionsgleichung von HRID 650715
[CH3:1][N:2]1[CH:6]2[CH2:7][CH:8]([OH:10])[CH2:9][CH:3]1[CH2:4][CH2:5]2.[C:11](Cl)(=[O:17])[CH2:12][CH2:13][C:14](Cl)=[O:15].[OH2:19].[OH-].[Na+]>C(Cl)Cl>[C:11]([O:17][CH:8]1[CH2:7][C@H:6]2[N:2]([CH3:1])[C@H:3]([CH2:4][CH2:5]2)[CH2:9]1)(=[O:19])[CH2:12][CH2:13][C:14]([O:10][CH:8]1[CH2:9][C@H:3]2[N:2]([CH3:1])[C@H:6]([CH2:5][CH2:4]2)[CH2:7]1)=[O:15]

Komponenten

6

Versuchsvorschrift

To a solution of 14.1 g (100 mmol) of tropine in 50 mL of methylene chloride is added dropwise 7.75 g (50 mmol) of succinyl chloride in 100 mL of methylene chloride with cooling in an ice bath. Then the mixture is allowed to warm to room temperature. After the reaction mixture is poured into 200 mL of cold water, the aqueous layer is adjusted to pH 10-11 with 6 N NaOH aqueous solution and extracted with chloroform. The resulting oil is purified by column chromatography (silica gel, 20% methanol in chloroform) to yield 11.8 g (65%) of bis-tropan-3-yl succinate as a thick oil.

Aufarbeitung

  1. temperaturewith cooling in an ice bath
  2. extractionextracted with chloroform
  3. customThe resulting oil is purified by column chromatography (silica gel, 20% methanol in chloroform)

Quellen und Nachweise

ORD-Eintrag
ord-c87e830c166943dab78312f30d7dbf6f
Quelldatensatz
uspto-grants-2001_08
Patentnummer
US06274757B1

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