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Chemical Structure| 91757-38-9 Chemical Structure| 91757-38-9

Structure of 91757-38-9

Chemical Structure| 91757-38-9

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Product Details of [ 91757-38-9 ]

CAS No. :91757-38-9
Formula : C8H18ClNO2
M.W : 195.69
SMILES Code : CC(C)[C@@H](C(OCC)=O)NC.[H]Cl

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Application In Synthesis of [ 91757-38-9 ]

* 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 [ 91757-38-9 ]

[ 91757-38-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 64-17-5 ]
  • [ 2480-23-1 ]
  • [ 91757-38-9 ]
YieldReaction ConditionsOperation in experiment
1.9 g With thionyl chloride; In neat (no solvent); for 16h;Reflux; To a solution of (2S)-3-methyl-2-(methylamino)butanoic acid (1.0 g, 7.6 mmol) in EtOH (10 mL) was added thionyl chloride (2.45 g, 21 mmol) dropwise at room temperature. The resulting mixture was stirred and refluxed for 16 hrs and then concentrated in vacuo. The residue was basified with saturated aqueous NaHC03 (30 mL) and extracted with DCM (50 mL) twice. The combined organic layer was washed with brine, dried over Na2S04 and concentrated in vacuo. The residue was dissolved in HCl/EtOAc (10 mL, 1 M) and concentrated to afford ethyl (2S)-3-methyl-2-(methylamino)butanoate hydrochloride (1.9 g, Compound AV-1) as a white solid.
1.9 g With thionyl chloride; for 16h;Reflux; To a solution of (2S)-3-methyl-2-(methylamino)butanoic acid (1.0 g, 7.6 mmol) in EtOH (10 mL) was added thionyl chloride (2.45 g, 21 mmol) dropwise at room temp erature. The resulting mixture was stirred and refluxed for 16 hrs and then concentrated in vacuo. The residue was basified with saturated aqueous NaHCO3 (30 mL) and extracted with DCM (50 mL) twice. The combined organic layer was washed with brine, dried over Na2SO4 and concentrated in vacuo. The residue was dissolved inHCIIEtOAc (10 mL, 1 M) and concentrated to afford ethyl (2S)-3-methyl-2- (methylamino)butanoate hydrochloride (1.9 g, Compound y-i) as a white solid.
1.9 g With thionyl chloride; for 16h;Reflux; To a solution of (2S)-3-methyl-2-(methylamino)butanoic acid (1.0 g, 7.6 mmol) in EtOH (10 mL) was added thionyl chloride (2.45 g, 21 mmol) dropwise at room temperature. The resulting mixture was stirred and refluxed for 16 hrs and then concentrated in vacuo. The residue was basified with saturated aqueous NaHCO3 (30 mL) and extracted with DCM (50 mL) twice. The combined organic layer was washed with brine, dried over Na2SO4 and concentrated in vacuo. The residue was dissolved in HCl/EtOAc (10 mL, 1 M) and concentrated to afford ethyl (2S)-3-methyl-2-(methylamino)butanoate hydrochloride (1.9 g, Compound AV-1) as a white solid.
 

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