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Sodium Hydroxide → 6-Phenyl-7-oxa-3-azabicyclo[4.1.0]heptane

HRID 895047
ノート
印刷プレビュー

反応式

HRID 895047 の反応式
BrBr.[Br-].[Na+].Br.[C:6]1([C:12]2[CH2:17][CH2:16][NH:15][CH2:14][CH:13]=2)[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.[OH-:18].[Na+]>O>[O:18]1[C:12]2([C:6]3[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=3)[CH:13]1[CH2:14][NH:15][CH2:16][CH2:17]2
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 14798Sodium HydroxideHCID 24408BromineHCID 253881Sodium BromideHCID 205741144-Phenyl-1,2,5,6-tetrahydropyridine hydrobromide

生成物 1

HCID 129293756-Phenyl-7-oxa-3-azabicyclo[4.1.0]heptane

試薬・触媒・溶媒 1

HCID 962Water溶媒2 回

実験手順

A solution of 33.6 g of bromine and 60 g of sodium bromide in 450 ml of water was added dropwise with stirring to solution comprising 50 g of 4-phenyl-1,2,5,6-tetrahydropyridine hydrobromide in 600 ml of water and the reaction mixture was then stirred at room temperature for 30 minutes. The solution was stirred on an ice bath while 252 ml of 10% sodium hydroxide was added dropwise thereto. The resulting mixture then being stirred at room temperature for a further 30 minutes. The aqueous solution was extracted with methylene chloride and the organic phase solution dried over sodium sulfate and then concentrated in vacuo to give 25.2 g of the desired 3,4-epoxy-4-phenyl piperidine as an oil.

後処理

  1. additionwas added dropwise
  2. stirringThe resulting mixture then being stirred at room temperature for a further 30 minutes
  3. extractionThe aqueous solution was extracted with methylene chloride
  4. dry with materialthe organic phase solution dried over sodium sulfate
  5. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-672e5faeeda843dba3654189040b632c
出典データセット
uspto-grants-1981_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04286095

反応ノート

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