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Chemical Structure| 934180-37-7 Chemical Structure| 934180-37-7

Structure of 934180-37-7

Chemical Structure| 934180-37-7

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Product Details of [ 934180-37-7 ]

CAS No. :934180-37-7
Formula : C13H23NO3
M.W : 241.33
SMILES Code : O=C(N1C2CC(O)CC1CCC2)OC(C)(C)C
MDL No. :MFCD30738066

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Application In Synthesis of [ 934180-37-7 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 934180-37-7 ]

[ 934180-37-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 24424-99-5 ]
  • [ 504-12-1 ]
  • [ 934180-37-7 ]
YieldReaction ConditionsOperation in experiment
83% With sodium hydroxide; In 1,4-dioxane; water; at -15 - 20℃; for 4.16667h; Crude enαto-9-azabicyclo[3.3.1]nonan-3-ol (from Step c) was dissolved in a solution of dioxane (500 ml_), water (187.5 ml.) and 4N sodium hydroxide (aq.) (62.5 ml.) and cooled to -15 0C under a nitrogen atmosphere. Di-terf-butyl dicarbonate (39.0 g, 0.18 mol) was added portionwise over 10 min, the reaction mixture allowed to warm to ambient temperature and stirring continued for 4 h during which time a white precipitate formed. EPO <DP n="16"/>Dioxane was evaporated under reduced pressure. Water (400 ml.) was added and the product extracted with dichloromethane (3 x 400 ml_). The organic phase was dried (MgSO4) and concentrated in vacuo to afford endo-3-hydroxy-9-azabicyclo[3.3.1]nonane- 9-carboxylic acid tert-butyl ester (24.0 g, 0.10 mol, 83% from enαto-9-benzyl-9- azabicyclo[3.3.1]nonan-3-ol) as a pale yellow solid.
83% With sodium hydroxide; In 1,4-dioxane; water; at -15 - 20℃; for 4.16667h; Crude <strong>[504-12-1]endo-9-azabicyclo[3.3.1]nonan-3-ol</strong> (from Step c) was dissolved in a solution of dioxane (500 mL), water (187.5 mL) and 4N sodium hydroxide (aq.) (62.5 mL) and cooled to -15 C. under a nitrogen atmosphere. Di-tert-butyl dicarbonate (39.0 g, 0.18 mol) was added portionwise over 10 min, the reaction mixture allowed to warm to ambient temperature and stirring continued for 4 h during which time a white precipitate formed. Dioxane was evaporated under reduced pressure. Water (400 mL) was added and the product extracted with dichloromethane (3 400 mL). The organic phase was dried (MgSO4) and concentrated in vacuo to afford endo-3-hydroxy-9-azabicyclo[3.3.1]nonane-9-carboxylic acid tert-butyl ester (24.0 g, 0.10 mol, 83% from endo-9-benzyl-9-azabicyclo[3.3.1]nonan-3-ol) as a pale yellow solid.
 

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