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

HRID 895047
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HRID 895047 반응식
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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

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

생성물 1

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

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-672e5faeeda843dba3654189040b632c
출처 데이터셋
uspto-grants-1981_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04286095

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