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(3-Bromopropyl)benzene → 4-(3-bromopropyl)benzoyl Chloride

HRID 346248
ノート
印刷プレビュー

反応式

HRID 346248 の反応式
[Br:1][CH2:2][CH2:3][CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.C(Cl)(=O)[C:12]([Cl:14])=[O:13].[Cl-].[Al+3].[Cl-].[Cl-]>ClC=C(Cl)Cl>[Br:1][CH2:2][CH2:3][CH2:4][C:5]1[CH:10]=[CH:9][C:8]([C:12]([Cl:14])=[O:13])=[CH:7][CH:6]=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 12503(3-Bromopropyl)benzeneHCID 65578Oxalyl chlorideHCID 6451240Aluminum(III) Chloride

生成物 1

HCID 113690154-(3-bromopropyl)benzoyl Chloride収率 97.3%

試薬・触媒・溶媒 1

HCID 6575Trichloroethylene溶媒

実験手順

To a cold (ice bath) stirred solution of 50.0 g (0.25 mole) of 1-bromo-3-phenylpropane (Aldrich) and 31.9 g (0.25 mole) of oxalyl chloride in 300 mL of trichloroethylene was added, portionwise, 33.3 g (0.25 mole) of aluminum chloride. The reaction mixture was stirred for 0.5 hr and then poured into ice water. The layers were separated and the aqueous layer was extracted with three 100 mL portions of methylene chloride. The combined organic layers were washed twice with 200 mL portions of water and dried (magnesium sulfate). The solvents were evaporated under reduced pressure to leave 63.6 g (97%) of 4-(3-bromopropyl)benzoyl chloride as an oil. To a solution of the acid chloride in 120 mL of dry benzene was added 60 mL of absolute ethanol and the mixture was heated at reflux for 3 hr. The solvents were evaporated under reduced pressure to give 63.4 g (93.5%) of an oil. The oil was purified by chromatography (3.5×90 cm glass column, 200 g of silica gel, benzene-hexane, 1:1). Fractions containing the desired component were combined and the solvents evaporated under reduced pressure to give 60.6 g (89%) of the title compound as a pale yellow oil.

後処理

  1. additionwas added
  2. customThe layers were separated
  3. extractionthe aqueous layer was extracted with three 100 mL portions of methylene chloride
  4. washThe combined organic layers were washed twice with 200 mL portions of water
  5. dry with materialdried (magnesium sulfate)
  6. customThe solvents were evaporated under reduced pressure

出典と根拠

ORDレコード
ord-7656ab29036248cd9fcb524e8e91563d
出典データセット
uspto-grants-1991_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05061720

反応ノート

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