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Benzylamine → (3R,4R)-1-benzyl-3,4-dihydroxypyrrolidine-2,5-dione

HRID 902859
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인쇄 미리보기

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HRID 902859 반응식
[C:1]([OH:10])(=O)[C@@H:2]([C@H:4]([C:6](O)=[O:7])[OH:5])[OH:3].[CH2:11]([NH2:18])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>C1(C)C(C)=CC=CC=1>[CH2:11]([N:18]1[C:6](=[O:7])[C@H:4]([OH:5])[C@@H:2]([OH:3])[C:1]1=[O:10])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1
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참가 물질

4

반응물 2

HCID 7504BenzylamineHCID 444305L-Tartaric acid

생성물 1

HCID 729946(3R,4R)-1-benzyl-3,4-dihydroxypyrrolidine-2,5-dione

시약·촉매·용매 1

HCID 7237O-Xylene용매

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온도
150 °C

실험 절차

L-Tartaric acid (30 g) and benzylamine (22 ml) were added to xylene (150 ml), and the mixture was heated under reflux at 150° C. for 3 hours using a Dean-Stark trap. After the reaction mixture was allowed to cool overnight, crystals were collected by filtration and washed with acetone. The resultant crude product was recrystallized from ethanol to obtain the title compound (23.2 g).

후처리

  1. temperaturethe mixture was heated
  2. temperatureto cool overnight
  3. filtrationcrystals were collected by filtration
  4. washwashed with acetone
  5. customThe resultant crude product was recrystallized from ethanol

출처 및 근거

ORD 기록
ord-b92a67768b5145719dccda173d76038a
출처 데이터셋
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07365205B2

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