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Propargyl bromide → 1-(1-Propylcyclobutyl)but-3-yn-1-ol

HRID 2249570
ノート
印刷プレビュー

反応式

HRID 2249570 の反応式
[CH2:1](Br)[C:2]#[CH:3].[Mg].[CH2:6]([C:9]1([CH:13]=[O:14])[CH2:12][CH2:11][CH2:10]1)[CH2:7][CH3:8]>CCOCC>[CH2:6]([C:9]1([CH:13]([OH:14])[CH2:3][C:2]#[CH:1])[CH2:12][CH2:11][CH2:10]1)[CH2:7][CH3:8]
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

5

反応物 3

HCID 7842Propargyl bromide2 回HCID 5462224MagnesiumHCID 143013561-Propylcyclobutane-1-carbaldehyde

生成物 1

HCID 142547761-(1-Propylcyclobutyl)but-3-yn-1-ol収率 250.6%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒2 回

反応条件

温度
40 °C

実験手順

Propargyl bromide (0.27 mL, 2.4 mmol) was added to a mixture of magnesium (1.1 g, 45 mmol) and mercuric chloride (30 mg, 0.117 mmol) in Et2O (60 mL). The mixture was warmed to 40° C. until bubbling commenced. The remainder of the propargyl bromide (2.1 mL, 19 mmol) was added in small portions. After −1.5 h the reaction became cloudy white. A solution of the aldehyde 3 (0.8 g, 7 mmol) in Et2O (4 mL) was added and the reaction was stirred for 16 h. The reaction was then quenched by cautiously adding saturated aqueous NH4Cl. The resultant mixture was extracted with Et2O. The organic portion was washed with brine, dried (MgSO4), filtered and concentrated in vacuo. FCC (silica gel, 1:1 pentane/CH2Cl2) gave 1.0 g (94%) of the alcohol 4.

後処理

  1. customuntil bubbling
  2. waitAfter −1.5 h the reaction became cloudy
  3. customThe reaction was then quenched by cautiously adding saturated aqueous NH4Cl
  4. extractionThe resultant mixture was extracted with Et2O
  5. washThe organic portion was washed with brine
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-81a15a3e8ff14f9bb438663efb15bd24
出典データセット
uspto-grants-2008_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07314890B2

反応ノート

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