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HCID 86750087、化合物 → (+)-cis-4-Amino-1-benzyl-3-methyl-2-oxopyrrolidine

HRID 1081693
ノート
印刷プレビュー

反応式

HRID 1081693 の反応式
[CH2:1]([N:8]1[CH2:12][C@H:11]([NH:13]C(OC(C)(C)C)=O)[C@H:10]([CH3:21])[C:9]1=[O:22])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>FC(F)(F)C(O)=O>[NH2:13][C@H:11]1[CH2:12][N:8]([CH2:1][C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[C:9](=[O:22])[C@H:10]1[CH3:21]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 86750087HCID 86750087、化合物

生成物 1

HCID 68547926(+)-cis-4-Amino-1-benzyl-3-methyl-2-oxopyrrolidine

試薬・触媒・溶媒 1

HCID 6422Trifluoroacetic acid溶媒

実験手順

In 15 ml of trifluoroacetic acid was dissolved 1.76 g of Compound (44). After 1 hour, the solution was concentrated under reduced pressure. To the residue was added 100 ml of water, and the mixture was washed with benzene. The aqueous layer was adjusted to a pH of 12 with sodium hydroxide and extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated to obtain the titled compound (45) as a colorless oil.

後処理

  1. concentrationthe solution was concentrated under reduced pressure
  2. additionTo the residue was added 100 ml of water
  3. washthe mixture was washed with benzene
  4. extractionextracted with chloroform
  5. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  6. customthe solvent was evaporated

出典と根拠

ORDレコード
ord-075ab613c908415697ab87f9396b4b0a
出典データセット
uspto-grants-1996_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05587386

反応ノート

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