ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Sodium Cyanide → 5-(2-Propyl-3,4-dichlorophenoxy)pentane nitrile

HRID 34970
ノート
印刷プレビュー

反応式

HRID 34970 の反応式
[CH2:1]([C:4]1[C:16]([Cl:17])=[C:15]([Cl:18])[CH:14]=[CH:13][C:5]=1[O:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11]Br)[CH2:2][CH3:3].[C-]#[N:20].[Na+]>CN(C)C=O>[CH2:1]([C:4]1[C:16]([Cl:17])=[C:15]([Cl:18])[CH:14]=[CH:13][C:5]=1[O:6][CH2:7][CH2:8][CH2:9][CH2:10][C:11]#[N:20])[CH2:2][CH3:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 8929Sodium CyanideHCID 212972695-(2-Propyl-3,4-dichlorophenoxy)pentyl bromide

生成物 1

HCID 212972585-(2-Propyl-3,4-dichlorophenoxy)pentane nitrile

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

A solution of 1.6 g. of 5-(2-propyl-3,4dichlorophenoxy)pentyl bromide and 0.22 g. of sodium cyanide were heated overnight at 75°-85° C. in 50 ml. of dimethylformamide. The solution was evaporated in vacuo and ethyl acetate and water were added to the residue. The layers were separated and the organic layer was washed several times with a saturated sodium chloride solution. The organic solution was filtered through sodium sulfate and evaporated to dryness to give 1.38 g. of the desired sub-title intermediate. NMR.

後処理

  1. customThe solution was evaporated in vacuo and ethyl acetate and water
  2. additionwere added to the residue
  3. customThe layers were separated
  4. washthe organic layer was washed several times with a saturated sodium chloride solution
  5. filtrationThe organic solution was filtered through sodium sulfate
  6. customevaporated to dryness
  7. customto give 1.38 g

出典と根拠

ORDレコード
ord-b9adf9d7b096468f83a8b7ace2b09bac
出典データセット
uspto-grants-1988_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04764521

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート