Maleimide → 4-(Tert.-butyloxycarbonylamino)-1,3-dioxo-1,3,3a,4,7,7a-hexahydroisoindole

HRID 128514ノート

反応式

HRID 128514 の反応式
[C:1]1(=[O:7])[NH:5][C:4](=[O:6])[CH:3]=[CH:2]1.[C:8]([O:12][C:13]([NH:15][CH:16]=[CH:17][CH:18]=[CH2:19])=[O:14])([CH3:11])([CH3:10])[CH3:9]>O1CCCC1>[C:8]([O:12][C:13]([NH:15][CH:16]1[CH:17]=[CH:18][CH2:19][CH:3]2[CH:2]1[C:1](=[O:7])[NH:5][C:4]2=[O:6])=[O:14])([CH3:10])([CH3:11])[CH3:9]

参加物

4

反応物 2

HCID 10935MaleimideHCID 22897234Tert-butyl N-buta-1,3-dienylcarbamate

生成物 1

HCID 193714494-(Tert.-butyloxycarbonylamino)-1,3-dioxo-1,3,3a,4,7,7a-hexahydroisoindole

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

48.0 g (0.5 mol) of maleimide are initially introduced into the reaction vessel as a solution in 200 ml of absolute tetrahydrofuran, and 120 g (0.5 mol) of approximately 70% strength 1-(tert.-butyloxycarbonylamino)-1,3-butadiene are added dropwise as a solution in 500 ml of absolute tetrahydrofuran, the temperature being kept at 20° to 30° C. The mixture is subsequently stirred overnight at room temperature. It is then concentrated and the residue is recrystallised from ethyl acetate. 57 g of product having a melting point of 177° to 182° C. are obtained. A further 13 g of melting point 158° to 160° C. are obtained from the mother liquor.

後処理

  1. custombeing kept at 20° to 30° C
  2. concentrationIt is then concentrated
  3. customthe residue is recrystallised from ethyl acetate
  4. customare obtained
  5. customA further 13 g of melting point 158° to 160° C. are obtained from the mother liquor

出典と根拠

ORDレコード
ord-37dd6bbf2b0c4f0ea822e3721e35198b
出典データセット
uspto-grants-1995_11
特許番号
US05464796

反応ノート

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