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Formaldehyde → (2R)-1-methylpyrrolidine-2-carboxylic acid

HRID 1014286
Notes
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Reaction equation

HRID 1014286 reaction equation
[NH:1]1[CH2:8][CH2:7][CH2:6][C@@H:2]1[C:3]([OH:5])=[O:4].[CH2:9]=O>O.[Pd]>[CH3:9][N:1]1[CH2:8][CH2:7][CH2:6][C@@H:2]1[C:3]([OH:5])=[O:4]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 2

HCID 712FormaldehydeHCID 8988D-Proline

Product 1

HCID 854034(2R)-1-methylpyrrolidine-2-carboxylic acidYield 40%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 962WaterSolvent

Conditions

Temperature
50 °C

Procedure

To a solution of D-proline (30 g, 260.7 mmol, 1 eq) and 37% aqueous formaldehyde (80.5 mL, 782 mmol, 3eq) in H2O (900 mL) was added 10% Pd/C (30 g) under N2. The mixture was stirred at 50° C. under H2 (30 psi) overnight. The mixture was heated to boiling and filtered to remove the catalyst. The solution was concentrated under reduced pressure, and then water (150 mL) was added to the mixture and concentrated, the procedure was repeated three times so as to remove unreacted formaldehyde. The crude product was resuspended in ACN/H2O (1:1, v/v) and lyophilized. The solid product was recrystallized from EtOH/acetone, filtered, liberally washed with acetone, and dried under reduced pressure to give 1-methyl-D-proline (12.3 g, 40%) as white solid. 1H NMR (400 MHz, MeOHD) δ ppm 1.95-1.99 (s, 1H), 2.1-2.2(s, 2H), 2.4-2.5 (m, 1H), 3.05-3.15(m,1H),3.3-3.35(s,1H),3.65-3.75(m, 1H),3.75-3.85(m,1H).

Workup

  1. temperatureThe mixture was heated
  2. filtrationfiltered
  3. customto remove the catalyst
  4. concentrationThe solution was concentrated under reduced pressure
  5. additionwater (150 mL) was added to the mixture
  6. concentrationconcentrated
  7. customto remove unreacted formaldehyde
  8. customThe solid product was recrystallized from EtOH/acetone
  9. filtrationfiltered
  10. washliberally washed with acetone
  11. customdried under reduced pressure

Sources & evidence

ORD record
ord-3bdf77bea1034da2b5db68daa1e9cae4
Source dataset
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07981903B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes