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Ammonium Chloride → 2-(1,3-Isoindolinedion-2-yl)-5-(2,2-dimethyl-3-methoxycarbonyl-propionyl)indane

HRID 1598561
ノート
印刷プレビュー

反応式

HRID 1598561 の反応式
C[Si]([N-][Si](C)(C)C)(C)C.[Li+].C([Li])CCC.[C:16]1(=[O:40])[C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[C:18](=[O:25])[N:17]1[CH:26]1[CH2:34][C:33]2[C:28](=[CH:29][CH:30]=[C:31]([C:35](=[O:39])[CH:36]([CH3:38])[CH3:37])[CH:32]=2)[CH2:27]1.Br[CH2:42][C:43]([O:45][CH3:46])=[O:44].[Cl-].[NH4+]>O1CCCC1>[C:16]1(=[O:40])[C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[C:18](=[O:25])[N:17]1[CH:26]1[CH2:34][C:33]2[C:28](=[CH:29][CH:30]=[C:31]([C:35](=[O:39])[C:36]([CH3:37])([CH3:38])[CH2:42][C:43]([O:45][CH3:46])=[O:44])[CH:32]=2)[CH2:27]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 25517Ammonium ChlorideHCID 60984Methyl bromoacetateHCID 2733832Lithium hexamethyldisilazaneHCID 189297332-(1,3-Isoindolinedion-2-yl)-5-(2-methylpropionyl)indaneHCID 178418339Butyllithium

生成物 1

HCID 189297382-(1,3-Isoindolinedion-2-yl)-5-(2,2-dimethyl-3-methoxycarbonyl-propionyl)indane
収率 51.3%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒3 回

反応条件

温度
-40 °C

実験手順

Lithium bis(trimethylsilyl)amide prepared from 1.78 g of 1,1,1,3,3,3-hexamethylsilazane and n-butyl lithium (6.9 ml of 1.6M hexane solution), dissolved in 50 ml of tetrahydrofuran was cooled to -40° C., and 3.30 g of 2-(1,3-isoindolinedion-2-yl)-5-(2-methylpropionyl)indane dissolved in 50 ml of tetrahydrofuran was added dropwise thereto over 15 minutes. The mixture was stirred at 0° C. for 20 minutes and cooled to -30° C. To the mixture was added dropwise 1.68 g of methyl bromoacetate dissolved in 10 ml of tetrahydrofuran, and the mixture was stirred at room temperature for 2.5 hours. To the reaction mixture was added a saturated ammonium chloride solution, the mixture was extracted with ethyl acetate, the extract was dried, and then the solvent was removed. The residue was purified by silica gel column chromatography (eluted by n-hexane:ethyl acetate =4:1). The resulting crystals were recrystallized from ethyl acetate-n-hexane to obtain 2.06 g of 2-(1,3-isoindolinedion-2-yl)-5-(2,2-dimethyl-3-methoxycarbonyl-propionyl)indane.

後処理

  1. additionwas added dropwise
  2. temperaturecooled to -30° C
  3. stirringthe mixture was stirred at room temperature for 2.5 hours
  4. extractionthe mixture was extracted with ethyl acetate
  5. customthe extract was dried
  6. customthe solvent was removed
  7. customThe residue was purified by silica gel column chromatography (eluted by n-hexane:ethyl acetate =4:1)
  8. customThe resulting crystals were recrystallized from ethyl acetate-n-hexane

出典と根拠

ORDレコード
ord-ddde2845c71f418cb8bc8fc2ed367554
出典データセット
uspto-grants-1998_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05739132

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート