Cyanide → 1,1'-Bipiperidine

HRID 2085074

反応式

HRID 2085074 の反応式
[C-:1]#[N:2].C[Mg+].[Br-].[CH2:6]1[CH2:10]O[CH2:8][CH2:7]1>CCOCC>[N:2]1([N:2]2[CH2:1][CH2:10][CH2:6][CH2:7][CH2:8]2)[CH2:1][CH2:10][CH2:6][CH2:7][CH2:8]1

参加物

5

反応条件

温度
25 °C

実験手順

The cyanide (4.87 g, 15 mmol) was taken up in THF (75 ml). CH3MgBr (25 ml of a 3.0 M solution in Et2O) was added to the reaction mixture at 0° C. The solution was allowed to warm to 25° C. and was stirred at that temperature for 18 h. The solution was partitioned between 25 wt % aqueous solution of sodium citrate and EtOAc. The aqueous layer was extracted with EtOAc. The combined EtOAc layers were washed with brine and dried (Na2SO4). Filtration and concentration gave a yellow oil. Purification via flash chromatography (95/5 to 90/10 EtOAc/MeOH. SiO2) gave 3.7 g (79%) of the piperidino-piperidine 12 as a yellow gum.

後処理

  1. customThe solution was partitioned between 25 wt % aqueous solution of sodium citrate and EtOAc
  2. extractionThe aqueous layer was extracted with EtOAc
  3. washThe combined EtOAc layers were washed with brine
  4. dry with materialdried (Na2SO4)
  5. filtrationFiltration and concentration
  6. customgave a yellow oil
  7. customPurification via flash chromatography (95/5 to 90/10 EtOAc/MeOH. SiO2)

出典と根拠

ORDレコード
ord-f2b30c5c7260423c9dbd8a1bbd1de431
出典データセット
uspto-grants-2004_04
特許番号
US06720325B2

関連ノート

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