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Bromine → (4-Bromopentyl)benzene

HRID 1706259
ノート
印刷プレビュー

反応式

HRID 1706259 の反応式
P(Br)(Br)(Br)(Br)Br.[Br:7]Br.P(Br)(Br)Br.[C:13]1([CH2:19][CH2:20][CH2:21][CH:22](O)[CH3:23])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>C(Cl)Cl.O>[Br:7][CH:22]([CH2:21][CH2:20][CH2:19][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[CH3:23]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 24408BromineHCID 24614Phosphorus tribromideHCID 62678Phosphorus pentabromideHCID 1027884-Hydroxy-1-phenylpentane

生成物 1

HCID 20487411(4-Bromopentyl)benzene

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 6344
Dichloromethane
溶媒
3 回

反応条件

温度
0 °C

実験手順

To a phosphorus pentabromide, prepared by addition of bromine (9.0 g.) in methylene chloride (10 ml.) to phosphorous tribromide (15.0 g.) in methylene chloride (15 ml.) at 0° C., is added 5-phenyl-2-pentanol (8.2 g.) in methylene chloride at 0° C. The mixture is stirred for 2.5 hours at 0° C. and is then allowed to warm to room temperature. Water (50 ml.) is added, the mixture stirred for one hour and the methylene chloride layer separated. The extraction is repeated and the combined extracts washed with water, saturated sodium bicarbonate solution, brine and then dried over magnesium sulfate. Concentration of the dried extracts gives 12.4 g. of title product as a light yellow oil.

後処理

  1. temperatureto warm to room temperature
  2. stirringthe mixture stirred for one hour
  3. customthe methylene chloride layer separated
  4. extractionThe extraction
  5. washthe combined extracts washed with water, saturated sodium bicarbonate solution, brine
  6. dry with materialdried over magnesium sulfate
  7. customConcentration of the dried extracts gives 12.4 g

出典と根拠

ORDレコード
ord-0845308433bd484493807e6bb94dc9ba
出典データセット
uspto-grants-1980_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04206225

反応ノート

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