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Hydrochloric Acid → 4-Oxo-4-(2-oxo-1-pyrrolidinyl)butyric acid

HRID 892610
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HRID 892610 반응식
[O:1]=[C:2]1[CH2:6][CH2:5][CH2:4][NH:3]1.[Li]CCCC.C1COCC1.[C:17]1(=[O:23])[O:22][C:20](=[O:21])[CH2:19][CH2:18]1.Cl>C1COCC1>[O:23]=[C:17]([N:3]1[CH2:4][CH2:5][CH2:6][C:2]1=[O:1])[CH2:18][CH2:19][C:20]([OH:22])=[O:21]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 7922Succinic anhydrideHCID 120252-PyrrolidoneHCID 178420697HCID 178420697, 화합물

생성물 1

HCID 148114614-Oxo-4-(2-oxo-1-pyrrolidinyl)butyric acid수율 86.6%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매
이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

반응 조건

온도
-30 °C

실험 절차

A solution of 2-oxopyrrolidine (5.00 g) in THF (60 ml) was cooled to -50° C., and a 1.55 M n-BuLi/THF solution (38 ml) was dropwise added thereto. After 0.5 hour's stirring at -30° C., succinic anhydride (6.00 g) was added dropwise, followed by stirring at a temperature of -30°--20° C. for 0.5 hour. The reaction mixture was poured into ice water and adjusted to pH 4 with 1N hydrochloric acid, and extracted with n-butanol. The organic layer was washed with saturated brine and concentrated to give 9.42 g of 4-oxo-4-(2-oxo-1-pyrrolidinyl)butyric acid.

후처리

  1. stirringby stirring at a temperature of -30°--20° C. for 0.5 hour
  2. extractionextracted with n-butanol
  3. washThe organic layer was washed with saturated brine
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-e2c53c4e4560415b87f66a7b4bb63786
출처 데이터셋
uspto-grants-1992_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05118811

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