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Chemical Structure| 60499-30-1 Chemical Structure| 60499-30-1

Structure of 60499-30-1

Chemical Structure| 60499-30-1

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Product Details of [ 60499-30-1 ]

CAS No. :60499-30-1
Formula : C12H17NO3S
M.W : 255.33
SMILES Code : CC1=CC=C(S(=O)(OC2CN(C)CC2)=O)C=C1
MDL No. :MFCD21097927

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Application In Synthesis of [ 60499-30-1 ]

* 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 [ 60499-30-1 ]

[ 60499-30-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 13220-33-2 ]
  • [ 98-59-9 ]
  • [ 60499-30-1 ]
YieldReaction ConditionsOperation in experiment
65% With potassium hydroxide; In tetrahydrofuran; at 0 - 25℃; for 16h; To the solution of l-methylpyrrolidin-3-ol (300 mg, 2.97 mmol, 1.00 equiv)and potassium hydroxide (666 mg, 11.86 mmol, 4.00 equiv) in tetrahydrofuran (5 mL) was added 4-methylbenzenesulfonyl chloride (848 mg, 4.45 mmol, 1.50 equiv) portion- wise maintaining the temperature at 0 °C and the resultant yellow slurry was stirred at 25 °C for 16 hours. The reaction mixture was filtered and the filtrate was concentrated in vacuo to afford the desired product as yellow oil (523 mg, 65percent) which was used without further purification; MS (ESI+) m/z 256.1 (M+H)+.
With triethylamine; In dichloromethane; Step 1: 1-Methyl-3-pyrrolidinyl 4-methylphenylsulfonate To a mixture of 3.0 g (0.03 mole) of <strong>[13220-33-2]3-hydroxy-1-methylpyrrolidine</strong>, 3.1 g (0.03 mole) of triethylamine, and 25 mL of methylene chloride was added 5.6 g (0.03 mole) of 4-methylphenylsulfonyl chloride, and the reaction mixture was stirred at room temperature for 3 hours. The reaction mixture was concentrated to a residue. The residue was dissolved in ether, the solution filtered, and the filtrate concentrated to give 5.75 g of product as an oil.
 

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