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Butanedioic acid, 2-acetyl-, 1,4-diethyl ester → ethyl (2,6-dimethyl-3H-pyrimidin-4-on-5yl)acetate

HRID 1440446
ノート
印刷プレビュー

反応式

HRID 1440446 の反応式
CC[O-].[Na+].Cl.[C:6]([NH2:9])(=[NH:8])[CH3:7].[C:10]([CH:13]([CH2:19][C:20]([O:22][CH2:23][CH3:24])=[O:21])[C:14](OCC)=[O:15])(=O)[CH3:11]>CCO>[CH3:7][C:6]1[NH:9][C:14](=[O:15])[C:13]([CH2:19][C:20]([O:22][CH2:23][CH3:24])=[O:21])=[C:10]([CH3:11])[N:8]=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 3

HCID 66197Butanedioic acid, 2-acetyl-, 1,4-diethyl esterHCID 67170Acetamidine monohydrochlorideHCID 2723922Sodium ethoxide

生成物 1

HCID 135459178ethyl (2,6-dimethyl-3H-pyrimidin-4-on-5yl)acetate

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A mixture of NaOEt (0.069 mol) in EtOH (prepared from 1.6 g of Na in 100 mL of EtOH), acetamidine hydrochloride (6.5 g, 0.069 mol), and diethyl 2-acetylsuccinate (15.0 g, 0.069 mol) was heated under reflux for 16 h. The mixture was concentrated, taken up in water (50 mL), and acidified with 2N HCl (12 mL). The aqueous mixture was extracted with CH2Cl2, and the extracts were dried (MgSO4) and concentrated. Trituration with either gave 3.9 g (27%) of product as a white solid, mp 175°177° C.

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

後処理

  1. temperaturewas heated
  2. temperatureunder reflux for 16 h
  3. concentrationThe mixture was concentrated
  4. extractionThe aqueous mixture was extracted with CH2Cl2
  5. dry with materialthe extracts were dried (MgSO4)
  6. concentrationconcentrated
  7. customwith either gave 3.9 g (27%) of product as a white solid, mp 175°177° C.

出典と根拠

ORDレコード
ord-f9ea8d5d93824e8992b5be7034fec426
出典データセット
uspto-grants-1996_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05498776

反応ノート

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