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 → Nonanenitrile, 3-hydroxy-, (3R)-

HRID 355295
ノート
印刷プレビュー

反応式

HRID 355295 の反応式
[C-:1]#[N:2].[Na+].Cl[CH2:5][C@H:6]([OH:13])[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]>CS(C)=O>[OH:13][C@H:6]([CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12])[CH2:5][C:1]#[N:2]
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 12575177(R)-1-chloro2-octanol

生成物 1

HCID 11298091Nonanenitrile, 3-hydroxy-, (3R)-収率 86.5%

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒2 回

実験手順

Under nitrogen atmosphere, 6.2 g (126 mM) of sodium cyanide and 50 ml of dimethyl sulfoxide (DMSO) were placed in two-necked round-bottomed flask and dissolved by heating, followed by stirring. The solution was left standing and a solution of 10.4 g of (R)-1-chloro2-octanol in 20 ml of DMSO was added dropwise to the solution at 50° C., followed by stirring for 20 hours at 50° C. After the reaction, distilled water was added to the reaction mixture, followed by extraction with diethyl ether. The organic layer was washed with distilled water and dried with anhydrous sodium sulfate, followed by distilling-off of the solvent under reduced pressure to obtain 8.48 g (54.7 mM) of (R)-3-hydroxynonanenitrile.

後処理

  1. dissolutiondissolved
  2. temperatureby heating
  3. waitThe solution was left
  4. stirringby stirring for 20 hours at 50° C
  5. customAfter the reaction
  6. distillationdistilled water
  7. additionwas added to the reaction mixture
  8. extractionfollowed by extraction with diethyl ether
  9. washThe organic layer was washed with distilled water
  10. dry with materialdried with anhydrous sodium sulfate

出典と根拠

ORDレコード
ord-414bf636e9a147d491a5e1acc25b937b
出典データセット
uspto-grants-1998_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05830386

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