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Chemical Structure| 1401102-93-9 Chemical Structure| 1401102-93-9

Structure of 1401102-93-9

Chemical Structure| 1401102-93-9

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Product Details of [ 1401102-93-9 ]

CAS No. :1401102-93-9
Formula : C12H13NO3
M.W : 219.24
SMILES Code : COC(C1CN(C2=CC=C(C=C2)C=O)C1)=O
English Name :Methyl 1-(4-formylphenyl)azetidine-3-carboxylate
MDL No. :MFCD27578564

Safety of [ 1401102-93-9 ]

Application In Synthesis of [ 1401102-93-9 ]

* 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 [ 1401102-93-9 ]

[ 1401102-93-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1355248-05-3 ]
  • [ 74-88-4 ]
  • [ 1401102-93-9 ]
YieldReaction ConditionsOperation in experiment
61% Stage #1: 1-(4-formylphenyl)azetidine-3-carboxylic acid With potassium carbonate In N,N-dimethyl-formamide at 0℃; for 0.166667h; Stage #2: methyl iodide at 0 - 20℃; for 2h; Inert atmosphere; 9 To a solution of 1 -(4-Formyl-phenyl)-azetidine-3-carboxylic acid(Preparation 8, 4g, 19.51 mmol) in DMF (50 mL) was added potassium carbonate (4.04g, 29.77 mmol) at 0 C and allowed to stir for 10 minutes followed by addition of methyl iodide (2.77g, 19.51 mmol) at 0 C. Resulting reaction mixture was stirred at room temperature for 2 hours under nitrogen atmosphere. After consumption of starting material, reaction mixture was quenched with ice cold water (150 mL) and extracted with EtOAc (3x150 mL). Combined organic layer was washed with water (2x300 mL), brine (250 mL), dried over sodium sulphate and evaporated under reduced pressure to afford brown colored semi solid (4.7g, crude). Crude was purified by column chromatography on silica gel (100-200 mesh). Compound was eluted using 20% ethyl acetate in hexane to afford yellow semisolid (2.6g, 61 %). 1H NMR (400 MHz, CDCI3) δ: 3.58-3.62 (m, 1 H), 3.76 (s, 3H), 4.15-4.22 (m, 4H), 6.42 (d, 2H, J = 8.6 Hz), 7.72 (d, 2H, J = 6.98 Hz), 9.74 (s, 1 H); LC-MS (M+H): = 220.20.
 

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