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Chemical Structure| 104016-82-2 Chemical Structure| 104016-82-2

Structure of 104016-82-2

Chemical Structure| 104016-82-2

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Product Details of [ 104016-82-2 ]

CAS No. :104016-82-2
Formula : C12H17NO3S
M.W : 255.33
SMILES Code : CS(=O)(OC1CN(CC2=CC=CC=C2)CC1)=O
English Name :1-Benzylpyrrolidin-3-yl methanesulfonate
MDL No. :MFCD20487884

Safety of [ 104016-82-2 ]

Application In Synthesis of [ 104016-82-2 ]

* 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 [ 104016-82-2 ]

[ 104016-82-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 124-63-0 ]
  • [ 775-15-5 ]
  • [ 104016-82-2 ]
YieldReaction ConditionsOperation in experiment
With dmap In acetonitrile at 0℃; for 0.166667h;
In dichloromethane at -20℃; for 1.5h; Intermediate 1 This tranformation was carried out via the method in J. L. Marco et.al. reference 96. Methanesulfonyl chloride (0.10 mol, 7.8 mL) was added slowly to a solution of racemic 1-benzyl-pyrolidin-3-ol (0.085 mol, 15 g) in 150 mL of dichloromethane which was stirring under a nitogen atmosphere at a temperature of -20° C. The reaction was stirred for an additional 1.5 h after addition was completed. The reaction was poured into a separatory funnel containing additional dichloromethane and washed with five thirty mL portions of saturated aqueous sodium bicarbonate. The organic layer was washed with one portion of water and then one portion of saturated aq NaCl. The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo to provide 22.75 g of crude mesylate which was used directly following characterization by proton NMR and LC/MS.
With triethylamine In toluene at 0 - 20℃; 1.G 1-benzyl-3-pyrrolidinyl methanesulfonate 1-Benzyl-3-pyrrolidinol (1.1 g) in toluene (10 mL) at 0° C. was treated with triethylamine (1 mL) and methanesulfonyl chloride (0.53 mL), warmed to room temperature, washed with saturated aqueous sodium bicarbonate, water, and brine, dried over anhydrous sodium sulfate, and concentrated. 1H NMR (300 MHz, DMSO-d6) δ 7.31 (s, 5H), 5.21 (m, 1H), 3.65 (q, 2H), 2.82 (m, 2H), 2.5 (m, 2H), 2.36 (m, 2H), 2.1 (m, 1H).
With triethylamine In dichloromethane at 0 - 20℃; Inert atmosphere;
4 g With triethylamine In dichloromethane at 20℃; for 1.5h; Cooling with ice; 6.1 Step 1: Preparation of 1-benzylpyrrolidin-3-yl methanesulfonate: 1-benzylpyrrolidin-3-ol (4 g, 1 eq) was dissolved in dichloromethane (40 mL), triethylamine (4 mL) was added, and methanesulfonyl chloride (1.5 eq) was added under ice bath, and then the temperature was raised to room temperature for reaction for 1.5 hours. Saturated sodium bicarbonate aqueous solution was added to adjust pH>10, and the aqueous phase was extracted with dichloromethane (30 mL×3), and the organic phase was washed with saturated brine, then dried over anhydrous sodium sulfate, and concentrated to obtain the target product (4 g).

 

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