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Methane → HCID 178524700、化合物

HRID 1042762
ノート
印刷プレビュー

反応式

HRID 1042762 の反応式
[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6](=[O:17])[C:7]([C:12]([O:14]CC)=[O:13])=[CH:8][NH:9]2)=[N:4][CH:3]=1.[OH-].[Na+].C>O>[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6]([OH:17])=[C:7]([C:12]([OH:14])=[O:13])[CH:8]=[N:9]2)=[N:4][CH:3]=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 297MethaneHCID 14798Sodium HydroxideHCID 13459134Ethyl 7-bromo-4-oxo-1,4-dihydro-1,5-naphthyridine-3-carboxylate

生成物 1

HCID 178524700HCID 178524700、化合物

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Ethyl 7-bromo-4-oxo-1,4-dihydro-1,5-naphthyridine-3-carboxylate (1 g, 3 mmol) and 2.5 M NaOH (10 mL) were refluxed for 1 h in a RBF fitted with a reflux condenser. The hot, heterogeneous mixture was diluted with boiling water at which point a tan precipitate dissolved. Charcoal was added to the solution, which was swirled for 2 min and then the mixture was filtered. Glacial acetic acid was added to the filtrate and a white precipitate started to form (pH adjusted to 4). The precipitate was filtered off upon cooling, washed with water and dried to provide the desired product as a white solid.

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. customfitted with a reflux condenser
  2. dissolutiondissolved
  3. filtrationthe mixture was filtered
  4. additionGlacial acetic acid was added to the filtrate
  5. customto form (pH adjusted to 4)
  6. filtrationThe precipitate was filtered off
  7. temperatureupon cooling
  8. washwashed with water
  9. customdried

出典と根拠

ORDレコード
ord-856a2398122641d887534ade4ff4ca3b
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08557816B2

反応ノート

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