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Ethylene → 8-Bromo-1,2,3,4-tetrahydronaphthalen-2-one

HRID 728074
ノート
印刷プレビュー

反応式

HRID 728074 の反応式
[Cl-].[Al+3].[Cl-].[Cl-].[Br:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[CH2:12][C:13](Cl)=[O:14].[CH2:16]=[CH2:17]>C(Cl)Cl>[Br:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:7]=1[CH2:12][C:13](=[O:14])[CH2:17][CH2:16]2
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 6325EthyleneHCID 41383862-Bromophenylacetyl chlorideHCID 6451240Aluminum(III) Chloride

生成物 1

HCID 41361878-Bromo-1,2,3,4-tetrahydronaphthalen-2-one

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

83.5 g of aluminum chloride (0.63 mmol) were introduced into 1.8 liters of methylene chloride at 0°-+5° C. 105 g (0.49 mole) of 2-bromophenyl-acetyl chloride (dissolved in 200 ml of methylene chloride) were added dropwise at 0°-+5° C. over 30 minutes. After stirring for 30 minutes at 0°-+5° C., 50 g of ethylene were passed in at such a rate that the reaction temperature did not exceed +10° C. The mixture was stirred for a further 2 hours at 20°-+25° C. The aluminum complex was decomposed by careful addition of 500 ml of ice water, the phases were separated, and the aqueous phase was extracted with 250 ml of methylene chloride. The title compound was obtained from the dried methylene chloride phase in a yield of 109 g as a yellow oil (content according to GC 97%) and employed without further purification.

後処理

  1. customdid not exceed +10° C
  2. stirringThe mixture was stirred for a further 2 hours at 20°-+25° C
  3. customthe phases were separated
  4. extractionthe aqueous phase was extracted with 250 ml of methylene chloride

出典と根拠

ORDレコード
ord-466ce25420ef495b813c28d665abd854
出典データセット
uspto-grants-1991_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05047422

反応ノート

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