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Chemical Structure| 1024038-31-0 Chemical Structure| 1024038-31-0

Structure of 1024038-31-0

Chemical Structure| 1024038-31-0

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Product Details of [ 1024038-31-0 ]

CAS No. :1024038-31-0
Formula : C7H14ClNO2
M.W : 179.64
SMILES Code : O=C(OC)C[C@@H]1CNCC1.[H]Cl
MDL No. :MFCD22377963
InChI Key :ZDVXNHFLFAPGGA-FYZOBXCZSA-N
Pubchem ID :67230738

Safety of [ 1024038-31-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 1024038-31-0 ]

* 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 [ 1024038-31-0 ]

[ 1024038-31-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 67-56-1 ]
  • [ 204688-60-8 ]
  • [ 1024038-31-0 ]
YieldReaction ConditionsOperation in experiment
(R)-methyl 2-(pyrrolidin-3-yl)acetate hydrochloride; <strong>[204688-60-8](R)-2-(1-(tert-butoxycarbonyl)pyrrolidin-3-yl)acetic acid</strong> (5.0 g, 21.81 mmol) in 4N HCl in dioxane (50 mL) was stirred at ambient temperature for 20 hours. The mixture was evaporated, coevaporated with dioxane (3×30 mL) and dried under high vacuum to give a yellow oil.This was dissolved in methanol (50 mL) at 10 C. and the solution saturated with HCl gas. The reaction mixture was then allowed to warm to ambient temperature and evaporated. The residue was co-evaporated with methanol (2×30 mL) and toluene (3×30 mL) and dried under high vacuum to give a yellow oil (4.0 g).1H NMR (400.13 MHz, DMSO-d6) delta 1.52-1.57 (1H, m), 2.063-2.13 (1H, m), 2.47-2.59 (3H, am), 2.7-2.8 (1H, m), 3.03-3.12 (1H, m), 3.14-3.25 (1H, m), 3.27-3.48 (3H, m), 3.61 (3H, s), 9.42 (2H, s)
 

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[ 1024038-31-0 ]

Esters

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Related Parent Nucleus of
[ 1024038-31-0 ]

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