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Methanol → Methyl 5-oxo-L-prolinate

HRID 21748
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HRID 21748 반응식
[NH:1]1[C:5](=[O:6])[CH2:4][CH2:3][C@H:2]1[C:7]([OH:9])=[O:8].CO.OS(O)(=O)=O.[C:17]([O-])(O)=O.[Na+]>C1COCC1>[CH3:17][O:8][C:7](=[O:9])[C@@H:2]1[CH2:3][CH2:4][C:5](=[O:6])[NH:1]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 887MethanolHCID 1118Sulfuric AcidHCID 7405L-Pyroglutamic AcidHCID 516892Sodium Bicarbonate

생성물 1

HCID 78646Methyl 5-oxo-L-prolinate

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
60 °C
이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

실험 절차

A 500 g sample of L-pyroglutamic acid was added to 2.8 L of anhydrous methanol, 28 mL of H2SO4 was added, and the mixture was stirred for 4 hr at 60° C. The reaction mixture was cooled to room temperature, 262 g of NaHCO3 was added, and the mixture was stirred for an additional 16 hr. The mixture was dried by addition of 314 g of Na2SO4 with stirring for 1 hr, then the mixture was filtered and the solvent was evaporated under vacuum to yield a pale yellow oil. The oil was dissolved in THF, and a small amount of unreacted acid was filtered off. The THF was removed under vacuum, and the residual oil was dried by azeotropic distillation with toluene.

후처리

  1. additionwas added
  2. temperatureThe reaction mixture was cooled to room temperature
  3. stirringthe mixture was stirred for an additional 16 hr
  4. dry with materialThe mixture was dried by addition of 314 g of Na2SO4
  5. stirringwith stirring for 1 hr
  6. filtrationthe mixture was filtered
  7. customthe solvent was evaporated under vacuum
  8. customto yield a pale yellow oil
  9. filtrationa small amount of unreacted acid was filtered off
  10. customThe THF was removed under vacuum
  11. dry with materialthe residual oil was dried by azeotropic distillation with toluene

출처 및 근거

ORD 기록
ord-0c770679fe32403da5c7fc2799431ed7
출처 데이터셋
uspto-grants-1995_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05424444

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