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Bromine → 3-Bromobicyclo[4.2.0]octa-1,3,5-triene

HRID 384300
ノート
印刷プレビュー

反応式

HRID 384300 の反応式
[C:1]12[CH2:8][CH2:7][C:6]=1[CH:5]=[CH:4][CH:3]=[CH:2]2.[Br:9]Br.S([O-])([O-])=O.[Na+].[Na+]>O.CCCCCC>[Br:9][C:3]1[CH:4]=[CH:5][C:6]2[CH2:7][CH2:8][C:1]=2[CH:2]=1
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 3

HCID 24408BromineHCID 24437Sodium SulfiteHCID 69667Benzocyclobutene

生成物 1

HCID 108669803-Bromobicyclo[4.2.0]octa-1,3,5-triene

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 8058Hexane溶媒

実験手順

Bicyclo[4.2.0]octa-1(6),2,4-triene 5a (7.9 g, 76 mmol) was dissolved in 80 mL of water at room temperature. Upon cooling by an ice-water, 3.9 mL of bromine was added dropwise. Upon completion of the addition, the ice-water bath was removed and the reaction mixture was warmed up to room temperature and stirred overnight. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was diluted with 50 mL of n-hexane and sodium sulfite (3 g, 23.8 mmol) was added. Upon completion of the addition, the mixture was stirred at room temperature for 30 minutes. Then the separated organic layer was dried over anhydrous sodium sulfate, filtered to remove the drying agent and concentrated under reduced pressure to obtain the title compound 3-bromo-bicyclo[4.2.0]octa-1(6),2,4-triene 5b (13.53 g) as a colourless oil, which was directly used in the next step.

後処理

  1. additionwas added dropwise
  2. additionUpon completion of the addition
  3. customthe ice-water bath was removed
  4. additionwas added
  5. additionUpon completion of the addition
  6. stirringthe mixture was stirred at room temperature for 30 minutes
  7. dry with materialThen the separated organic layer was dried over anhydrous sodium sulfate
  8. filtrationfiltered
  9. customto remove the drying agent
  10. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-73979fc817a84d85b6a6ad105883c357
出典データセット
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08367710B2

反応ノート

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