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Cumene → (S)-1-benzyl-3-hydroxypyrrolidine-2,5-dione

HRID 1081433
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HRID 1081433 반응식
[C:1]([OH:9])(=O)[C@H:2]([CH2:4][C:5](O)=[O:6])[OH:3].[CH2:10]([NH2:17])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.C1(C(C)C)C=CC=CC=1>O>[CH2:10]([N:17]1[C:5](=[O:6])[CH2:4][C@H:2]([OH:3])[C:1]1=[O:9])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7406CumeneHCID 7504BenzylamineHCID 222656L-Malic Acid

생성물 1

HCID 10954694(S)-1-benzyl-3-hydroxypyrrolidine-2,5-dione수율 39.6%

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

A mixture of 50.0 g (0.373 mole) (S)-malic acid (Ia), 41 ml (0.373 mole) benzyl amine and 250 ml cumene was heated with an internal temperature of 155° C. for 2.5 h on a water separator, during which time 12 ml water were separated. An oily phase formed during cooling off which slowly crystallized. The cumene was decanted off thereafter and the residue crystallized out of 220 ml EtOH. 30.3 g (39.6%) (S)-1-benzyl-3-hydroxy-2,5-pyrrolidinedione (IIa) were isolated in the form of colorless crystals.

후처리

  1. customwere separated
  2. customAn oily phase formed
  3. temperatureduring cooling off which
  4. customslowly crystallized
  5. customThe cumene was decanted off
  6. customthe residue crystallized out of 220 ml EtOH

출처 및 근거

ORD 기록
ord-b610e96e4bf14fa2b45f8c820a93921d
출처 데이터셋
uspto-grants-1996_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05585500

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