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Sodium Hydroxide → 4-Pyrrolidinopyridine

HRID 652562
ノート
印刷プレビュー

反応式

HRID 652562 の反応式
[Cl-].C(CC[N+:7]1[CH:12]=[CH:11][C:10](C#N)=[CH:9][CH:8]=1)(=O)N.[NH:15]1[CH2:19][CH2:18][CH2:17][CH2:16]1.[OH-].[Na+].[OH-].[Na+]>O>[N:15]1([C:10]2[CH:9]=[CH:8][N:7]=[CH:12][CH:11]=2)[CH2:19][CH2:18][CH2:17][CH2:16]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 14798Sodium HydroxideHCID 159190721-(3-Amino-3-oxopropyl)-4-cyanopyridin-1-ium chlorideHCID 21292233Pyrrolidine sodium hydroxide

生成物 1

HCID 755674-Pyrrolidinopyridine

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A solution of 1-(2-carbamoylethyl)-4-cyanopyridinium chloride (21.2 g; 0.1 mole) dissolved in 15 ml of deionized water was prepared and charged to the dropping funnel. This solution was then added to the pyrrolidine/sodium hydroxide solution at a rate which permitted maintenance of the reaction temperature with stirring at below 5° C. It was held there for an additional hour, after which 14 g (0.175 mole) of a 50% (w/w) sodium hydroxide solution was added dropwise with continued maintenance of the reaction temperature below 5° C. (approximately 45 minutes). The mixture was then heated to reflux and maintained for two hours and then allowed to cool.

後処理

  1. customwas prepared
  2. additioncharged to the dropping funnel
  3. waitIt was held there for an additional hour
  4. temperatureThe mixture was then heated
  5. temperatureto reflux
  6. temperaturemaintained for two hours
  7. temperatureto cool

出典と根拠

ORDレコード
ord-52dd917cfa1643d28d8a875824241ce3
出典データセット
uspto-grants-1987_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04672121

反応ノート

読み込み中…

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