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Diethyl Oxalate → HCID 86709894、化合物

HRID 929483
ノート
印刷プレビュー

反応式

HRID 929483 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[NH:8][C:9](=[O:17])[CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.C([O:20][C:21](=O)[C:22](OCC)=[O:23])C.CC(C)([O-])C.[K+]>O>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[N:8]1[C:9](=[O:17])[C:10]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[C:22]([OH:23])[C:21]1=[O:20]
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 3

HCID 7268Diethyl OxalateHCID 364845N-(2-Chlorophenyl)-2-phenylacetamideHCID 23665647Potassium tert-butoxide

生成物 1

HCID 86709894HCID 86709894、化合物

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

After the addition of anhydride THF (20 ml) to compound 5b (1.40 g, 7.34 mmol), the temperature was adjusted to 0° C. Diethyloxalate (1.45 g, 9.50 mmol) and potassium t-butoxide (1.35 g, 11.9 mmol) were added thereto and the agitation for 3 hours was carried out. After the identification of the reaction progress with TLC, the solution was poured into the distilled water and acidified with 1N HCL aqueous solution. Three times extractions were carried out with EA and three times washings were carried out with brine. Water was removed by using Na2SO4, solvents were removed and then, crude purification was carried out by the column chromatography (EA/HX, ⅕).

後処理

  1. customwas adjusted to 0° C
  2. extractionThree times extractions
  3. customWater was removed
  4. customwere removed
  5. customcrude purification

出典と根拠

ORDレコード
ord-f51ae69204c24faeaa80f428f5bee4af
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09296690B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート