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Ethyl cyclohexanoate → Ethyl 5,6,7,8-tetrahydroquinoline-6-carboxylate

HRID 2265138
ノート
印刷プレビュー

反応式

HRID 2265138 の反応式
[CH2:1]1[CH2:6][CH2:5][CH:4]([C:7]([O:9][CH2:10][CH3:11])=[O:8])[CH2:3][CH2:2]1.[CH2:12]([NH2:15])[C:13]#[CH:14]>O.O.[Na+].Cl[Au-](Cl)(Cl)Cl.C(O)C>[N:15]1[C:1]2[CH2:6][CH2:5][CH:4]([C:7]([O:9][CH2:10][CH3:11])=[O:8])[CH2:3][C:2]=2[CH:14]=[CH:13][CH:12]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 18686Ethyl cyclohexanoateHCID 239041Propargylamine

生成物 1

HCID 23157133Ethyl 5,6,7,8-tetrahydroquinoline-6-carboxylate

試薬・触媒・溶媒 2

HCID 18949434Sodium tetrachloroaurate dihydrate触媒HCID 702Ethanol溶媒2 回

実験手順

At 60° C., ethanol (250 mL) solution of 500 g of ethyl 4-cyclohexanecarboxylate is added to ethanol (2.5 L) solution of 376 mL of propargylamine and 29.2 g of sodium tetrachloroaurate(III) dihydrate, and stirred overnight with reflux. The insoluble solid substance was removed through filtration through Celite, and the solvent was evaporated off under reduced pressure. The residue was separated and purified through silica gel column chromatography (hexane/ethyl acetate=1/1) to obtain 555 g of ethyl 5,6,7,8-tetrahydroquinoline-6-carboxylate as a brown oily substance. The compound contained impurities.

後処理

  1. temperaturewith reflux
  2. customThe insoluble solid substance was removed through filtration through Celite
  3. customthe solvent was evaporated off under reduced pressure
  4. customThe residue was separated
  5. custompurified through silica gel column chromatography (hexane/ethyl acetate=1/1)

出典と根拠

ORDレコード
ord-a40a67b9dcb0485d9e742f887b3cc8c8
出典データセット
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07855294B2

反応ノート

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