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

1,2-Dibromoethane → 1-(6-Chloropyridazin-3-yl)cyclopropane-1-carbonitrile

HRID 1425958
ノート
印刷プレビュー

反応式

HRID 1425958 の反応式
[OH-].[Na+].[Cl:3][C:4]1[N:9]=[N:8][C:7]([CH2:10][C:11]#[N:12])=[CH:6][CH:5]=1.Br[CH2:14][CH2:15]Br>[Cl-].C([N+](CCCC)(CCCC)CCCC)C1C=CC=CC=1.C(#N)C>[Cl:3][C:4]1[N:9]=[N:8][C:7]([C:10]2([C:11]#[N:12])[CH2:15][CH2:14]2)=[CH:6][CH:5]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 78391,2-DibromoethaneHCID 14798Sodium HydroxideHCID 224447672-(6-Chloropyridazin-3-yl)acetonitrile

生成物 1

HCID 866961331-(6-Chloropyridazin-3-yl)cyclopropane-1-carbonitrile

試薬・触媒・溶媒 2

HCID 159952Benzyltributylammonium chloride触媒HCID 6342Acetonitrile
溶媒

実験手順

Aqueous NaOH solution (50%, 5 mL) was added to a solution of (6-chloro-pyridazin-3-yl)-acetonitrile (0.21 g), 1,2-dibromoethane (0.14 mL), and benzyltributylammonium chloride (0.43 g) in acetonitrile (5 mL) at room temperature. The resulting mixture was stirred at room temperature for 4 h and was then extracted with ethyl acetate. The combined extracts were washed with brine and dried (MgSO4). The solvent was evaporated and the residue was chromatographed on silica gel (cyclohexane/ethyl acetate 1:1→0:1) to give the title compound as a solid. Yield: 0.14 g (57% of theory); LC (method 1): tR=1.12 min; Mass spectrum (ESI+): m/z=180/182 (Cl) [M+H]+.

後処理

  1. extractionwas then extracted with ethyl acetate
  2. washThe combined extracts were washed with brine
  3. dry with materialdried (MgSO4)
  4. customThe solvent was evaporated
  5. customthe residue was chromatographed on silica gel (cyclohexane/ethyl acetate 1:1→0:1)

出典と根拠

ORDレコード
ord-5b6e4df7583b4decae2c8ab8d784585f
出典データセット
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08933072B2

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