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Formaldehyde → (R)-Methyl 1-methylpyrrolidine-2-carboxylate

HRID 644022
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HRID 644022 반응식
S(=O)(=O)(O)O.[NH:6]1[CH2:13][CH2:12][CH2:11][C@@H:7]1[C:8]([OH:10])=O.[C:14](=O)([O-])[O-].[K+].[K+].[CH2:20]=[O:21].[BH4-].[Na+]>CO>[CH3:20][O:21][C:8]([C@H:7]1[CH2:11][CH2:12][CH2:13][N:6]1[CH3:14])=[O:10]
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참가 물질

7

반응물 5

HCID 712FormaldehydeHCID 1118Sulfuric AcidHCID 8988D-ProlineHCID 11430Potassium CarbonateHCID 4311764Sodium borohydride

생성물 1

HCID 20803296(R)-Methyl 1-methylpyrrolidine-2-carboxylate

시약·촉매·용매 1

HCID 887
Methanol
용매

실험 절차

To a solution of sulfuric acid (3.5 ml, 65.3 mmol) in methanol (45 ml) was added D-proline (10.0 g, 86.9 mmol). The mixture was refluxed with stirring for 18 h. The solution was then cooled to 0° C. and neutralised by addition of aqueous potassium carbonate (2.5 M; 10 ml). Formaldehyde (37% solution in water; 11 ml, 136 mmol) was added and the mixture stirred at 0° C. for 15 minutes. Sodium borohydride (1.6 g, 42.3 mmol) was added at 0° C. and the mixture was stirred at room temperature for 3 h. The precipitate was filtered off and the filtrate was partitioned between dichloromethane and water. The isolated aqueous layer was adjusted to pH 10 using solid sodium carbonate and extracted with dichloromethane. The combined organic layers were dried over sodium sulfate and concentrated in vacuo to afford crude (R)-1-methylpyrrolidine-2-carboxylic acid methyl ester (13.13 g).

후처리

  1. temperatureThe mixture was refluxed
  2. stirringthe mixture stirred at 0° C. for 15 minutes
  3. stirringthe mixture was stirred at room temperature for 3 h
  4. filtrationThe precipitate was filtered off
  5. customthe filtrate was partitioned between dichloromethane and water
  6. extractionextracted with dichloromethane
  7. dry with materialThe combined organic layers were dried over sodium sulfate
  8. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-793bf44297054be58a442f73a9974de4
출처 데이터셋
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07700634B2

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