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Chemical Structure| 146257-05-8 Chemical Structure| 146257-05-8

Structure of 146257-05-8

Chemical Structure| 146257-05-8

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Product Details of [ 146257-05-8 ]

CAS No. :146257-05-8
Formula : C11H21NO3
M.W : 215.29
SMILES Code : O=C(N1CC(COC)CC1)OC(C)(C)C
English Name :tert-Butyl 3-(methoxymethyl)pyrrolidine-1-carboxylate
MDL No. :MFCD21143151

Safety of [ 146257-05-8 ]

Application In Synthesis of [ 146257-05-8 ]

* 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 [ 146257-05-8 ]

[ 146257-05-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 122684-33-7 ]
  • [ 146257-05-8 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: lithium aluminium tetrahydride / diethyl ether / -78 °C 2: potassium carbonate / N,N-dimethyl-formamide
  • 2
  • [ 114214-69-6 ]
  • [ 74-88-4 ]
  • [ 146257-05-8 ]
YieldReaction ConditionsOperation in experiment
60 % With potassium carbonate In N,N-dimethyl-formamide 1.1 Synthesis of 3-methoxymethyl-pyrrolidine-1H hydrochloride: 1-Boc-3-hydroxymethylpyrrolidine (1.0 g, 1.0 equiv.) and CH3I (0.84 g, 1.2 equiv.) were added to a DMF solution (6 mL) containing potassium carbonate (1.38 g, 2.0 equiv.) and reacted overnight to obtain 0.64 g of 3-methoxymethyl-pyrrolidine-1-carboxylic acid tert-butyl ester (or 3-methoxymethyl-pyrrolidine-1-Boc), with a yield of 60%. At room temperature and nitrogen, thionyl chloride (1 mL, 2.9 equiv.) was added dropwise to a solution of 3-methoxymethyl-pyrrolidine-1-carboxylic acid tert-butyl ester (1.03 g, 1.0 equiv.) in methanol (25 mL). The reaction mixture was refluxed for 2 hours and cooled at room temperature. The reaction mixture was concentrated and the crude product was dissolved in dichloromethane. The solution was concentrated to give 0.79 g (100%) of 3-methoxymethyl-pyrrolidine-1H hydrochloride as an off-white solid.
 

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