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

2-Butyne-1,4-diol → (4-Hydroxy-but-2-ynyloxy)-acetonitrile

HRID 349368
ノート
印刷プレビュー

反応式

HRID 349368 の反応式
[H-].[Na+].[CH2:3]([OH:8])[C:4]#[C:5][CH2:6][OH:7].Br[CH2:10][C:11]#[N:12]>C1COCC1>[OH:7][CH2:6][C:5]#[C:4][CH2:3][O:8][CH2:10][C:11]#[N:12]
参加物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 80662-Butyne-1,4-diolHCID 11534BromoacetonitrileHCID 24758Sodium hydride

生成物 1

HCID 86012515(4-Hydroxy-but-2-ynyloxy)-acetonitrile収率 29%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

Sodium hydride (60% dispersion in oil, 7.5 g, 188 mmol) was added to a solution of 2-butyne-1,4-diol (16.1 g, 187 mmol) in THF (150 mL) at 0° C. under nitrogen. After 1 h at 0° C., bromoacetonitrile (8.33 mL, 120 mmol) was added slowly and the reaction was allowed to warm to rt. After 22 h at rt, the reaction was quenched with 1 N HCl (150 mL) and extracted with EtOAc (3×150 mL). The combined extracts were washed with brine (150 mL), dried (Na2SO4), filtered and concentrated in vacuo. Purification of the residue by flash column chromatography on silica gel (CH2Cl2→2% MeOH/CH2Cl2, gradient) afforded 4.35 g (29%) of (4-hydroxy-but-2-ynyloxy)-acetonitrile.

後処理

  1. waitAfter 22 h at rt
  2. customthe reaction was quenched with 1 N HCl (150 mL)
  3. extractionextracted with EtOAc (3×150 mL)
  4. washThe combined extracts were washed with brine (150 mL)
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customPurification of the residue by flash column chromatography on silica gel (CH2Cl2→2% MeOH/CH2Cl2, gradient)

出典と根拠

ORDレコード
ord-a0263dc918064c5f93fc19fbc61dc920
出典データセット
uspto-grants-2007_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07179820B2

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