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

HRID 1014286
ノート
印刷プレビュー

反応式

HRID 1014286 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 712FormaldehydeHCID 8988D-Proline

生成物 1

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

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 962Water溶媒

反応条件

温度
50 °C

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-3bdf77bea1034da2b5db68daa1e9cae4
出典データセット
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07981903B2

反応ノート

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