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

HRID 1014286
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HRID 1014286 반응식
[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]
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참가 물질

5

반응물 2

HCID 712FormaldehydeHCID 8988D-Proline

생성물 1

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

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 962Water용매

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온도
50 °C

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-3bdf77bea1034da2b5db68daa1e9cae4
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07981903B2

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