Water → Bis(tropan-3-yl) succinate

HRID 842757Notes

Reaction equation

HRID 842757 reaction equation
[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]

Participants

6

Reactant 4

HCID 962WaterHCID 84248-Methyl-8-azabicyclo(3.2.1)octan-3-olHCID 10970Succinyl chlorideHCID 14798Sodium Hydroxide

Product 1

HCID 11824654Bis(tropan-3-yl) succinateYield 65%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent2×

Procedure

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.

Workup

  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)

Sources & evidence

ORD record
ord-cdd283966d724d0bbd6fb6954197270b
Source dataset
uspto-grants-2002_04
Patent number
US06376510B1

Reaction notes

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