Methanol → (S)-Methyl 1-methylpyrrolidine-2-carboxylate

HRID 21747Notes

Reaction equation

HRID 21747 reaction equation
[CH3:1][N:2]1[CH2:9][CH2:8][CH2:7][C@H:3]1[C:4]([OH:6])=[O:5].S(Cl)(Cl)=O.[CH3:14]O>>[CH3:14][O:5][C:4](=[O:6])[C@@H:3]1[CH2:7][CH2:8][CH2:9][N:2]1[CH3:1]

Participants

4

Reactant 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 643474N-Methyl-L-proline

Product 1

HCID 10920622(S)-Methyl 1-methylpyrrolidine-2-carboxylate

Procedure

To a solution of N-methyl (L)-proline, from step 3a, in methanol at 0° C. is added thionyl chloride (1.1 eq) dropwise, and the reaction mixture is slowly allowed to warm to room temperature. Upon completion of the reaction the solvent is removed in vacuo, and the crude product is dissolved in 10% aq. HCl and washed with ether. The aqueous layer is adjusted to pH--12 with K2CO3 (solid) and extracted with CH2Cl2. The combined CH2Cl2 layers are dried (MgSO4) and concentrated to afford the crude product as a clear oil.

Workup

  1. customUpon completion of the reaction the solvent
  2. customis removed in vacuo
  3. dissolutionthe crude product is dissolved in 10% aq. HCl
  4. washwashed with ether
  5. extraction12 with K2CO3 (solid) and extracted with CH2Cl2
  6. dry with materialThe combined CH2Cl2 layers are dried (MgSO4)
  7. concentrationconcentrated

Sources & evidence

ORD record
ord-88f6c2704c064f2a878dc8c470c3f1f8
Source dataset
uspto-grants-1995_06
Patent number
US05424444

Reaction notes

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