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Diethylaluminum chloride → HCID 21892018、化合物

HRID 1826847
ノート
印刷プレビュー

反応式

HRID 1826847 の反応式
[CH3:1][C:2]1[C:3](=[O:23])[N:4]2[C:16](=[CH:17][C:18]=1[C:19](=[O:22])[CH2:20][CH3:21])[C:7]1=[N:8][C:9]3[C:14]([CH:15]=[C:6]1[CH2:5]2)=[CH:13][CH:12]=[CH:11][CH:10]=3.Cl[Al](CC)CC.Br[CH2:31][C:32]([O:34][CH2:35][CH3:36])=[O:33].[K].C(C(C(C([O-])=O)O)O)([O-])=O.[Na+].[Na+]>O1CCCC1.[Zn].C([O-])(=O)C.[Ag+].C(O)C>[OH:22][C:19]([C:18]1[CH:17]=[C:16]2[N:4]([CH2:5][C:6]3[C:7]2=[N:8][C:9]2[C:14]([CH:15]=3)=[CH:13][CH:12]=[CH:11][CH:10]=2)[C:3](=[O:23])[C:2]=1[CH3:1])([CH2:20][CH3:21])[CH2:31][C:32]([O:34][CH2:35][CH3:36])=[O:33]
参加物実験手順後処理出典と根拠反応ノート

参加物

10

反応物 5

HCID 7277Diethylaluminum chlorideHCID 7748Ethyl bromoacetateHCID 13355Disodium 2,3-dihydroxybutanedioateHCID 1940068-Methyl-7-propanoylindolizino[1,2-b]quinolin-9(11H)-oneHCID 5462222Potassium

生成物 1

HCID 21892018HCID 21892018、化合物収率 16.6%

試薬・触媒・溶媒 4

HCID 11246Silver acetate触媒HCID 23994Zinc触媒HCID 702Ethanol溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

A suspension of zinc (1.25 g, 19.1 mmol), 8-methyl-7-propionylindolizino[1,2-b]quinoline-9-(11H)-one (500 mg, 1.43 mmol, as obtained by Kingsburry, W. D., Tetrahedron Lett. 29:6847 (1988)) and silver acetate (250 mg, 1.50 mmol) in anhydrous tetrahydrofuran (10 ml) is agitated at ambient temperature under an argon atmosphere. After 10 minutes, the reaction mixture is activated by the dropwise addition of a molar solution of chlorodiethylaluminium (10 ml, 10 mmol), then ethyl bromoacetate (1.25 ml, 11.3 mmol) is added dropwise and the resultant mixture is left to react for another 5 hours. The reaction is stopped by the successive addition of ethyl alcohol (10 ml) and a saturated solution of potassium and sodium tartrate (10 ml). The resultant mixture is agitated for another hour, filtered and concentrated under reduced pressure. The residue is taken up in dichloromethane (30 ml), washed with water, dried, concentrated and purified by column chromatography (SiO2, CH2Cl2/MeOH:98/2), which produces 93 mg (1.5%) of desired product in the form of a pale yellow solid, m.p. 185–188° C.

後処理

  1. customto react for another 5 hours
  2. filtrationfiltered
  3. concentrationconcentrated under reduced pressure
  4. washwashed with water
  5. customdried
  6. concentrationconcentrated
  7. custompurified by column chromatography (SiO2, CH2Cl2/MeOH:98/2), which

出典と根拠

ORDレコード
ord-4c3de40671814d11b0d7aeae19544390
出典データセット
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07053102B2

反応ノート

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