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Water → 2-Pentylcyclopentanecarbonitrile

HRID 1674451
ノート
印刷プレビュー

反応式

HRID 1674451 の反応式
S([CH2:11][N+:12]#[C-])(C1C=CC(C)=CC=1)(=O)=O.[CH2:14]([CH:19]1[CH2:23][CH2:22][CH2:21][C:20]1=O)[CH2:15][CH2:16][CH2:17][CH3:18].C(O[K])(C)(C)C.O>COCCOC.C(O)C>[CH2:14]([CH:19]1[CH2:23][CH2:22][CH2:21][CH:20]1[C:11]#[N:12])[CH2:15][CH2:16][CH2:17][CH3:18]
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 962WaterHCID 209592-Pentylcyclopentan-1-oneHCID 161915Tosylmethyl isocyanideHCID 178418922HCID 178418922、化合物

生成物 1

HCID 673394172-Pentylcyclopentanecarbonitrile収率 58.7%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒
HCID 8071
1,2-Dimethoxyethane
溶媒

反応条件

温度
0 °C

実験手順

27.6 g of tosylmethyl isocyanide and 17 g of 2-pentylcyclopentanone were dissolved in 400 ml of 1,2-dimethoxyethane and 10 ml of ethanol. The solution was cooled to 0° C. with an ice-bath, and 29 g of tBuOK were added in 1 hour maintaining the temperature between 0 and 10° C. After completion of the reaction, the reaction mixture was poured into water and extracted with cyclohexane. The organic layer was washed 3 times with water until neutral pH. Purification by bulb-to-bulb distillation (130° C./0.06 mbar) gave 10.7 g of the pure 2-pentylcyclopentanecarbonitrile.

後処理

  1. temperaturemaintaining the temperature between 0 and 10° C
  2. customAfter completion of the reaction
  3. extractionextracted with cyclohexane
  4. washThe organic layer was washed 3 times with water until neutral pH
  5. customPurification
  6. distillationby bulb-to-bulb distillation (130° C./0.06 mbar)

出典と根拠

ORDレコード
ord-c49271624cf74a5784767b8842038fd4
出典データセット
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08003084B2

反応ノート

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