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

Acetyl chloride → 5-Formylaminomethyl-3-methylisoxazole

HRID 1196858
ノート
印刷プレビュー

反応式

HRID 1196858 の反応式
[N+:1]([CH2:4][CH3:5])([O-:3])=O.C[O-].[Na+].[Na].C(Cl)(=O)C.[CH:14]([NH:16][CH2:17][C:18]#[CH:19])=[O:15]>CN(C)C(=O)C.CO>[CH:14]([NH:16][CH2:17][C:18]1[O:3][N:1]=[C:4]([CH3:5])[CH:19]=1)=[O:15]
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

8

反応物 5

HCID 6367Acetyl chlorideHCID 6587NitroethaneHCID 5360545SodiumHCID 9855445N-(prop-2-yn-1-yl)formamideHCID 10942334Sodium Methoxide

生成物 1

HCID 179326965-Formylaminomethyl-3-methylisoxazole

試薬・触媒・溶媒 2

HCID 887
Methanol
溶媒
HCID 31374Dimethylacetamide溶媒2 回

反応条件

温度
5 °C

実験手順

A stirred solution of nitroethane (17.9 ml, 0.25 mol) in N,N-dimethylacetamide (DMA) (250 ml) was added dropwise at 25°-30° C. to a solution of sodium methoxide, prepared by dissolving sodium (5.75 g) in dry methanol. The reaction mixture was cooled to 5° C. and acetyl chloride (18.5 ml, 0.26 mol) was added at 5°-10° C. Then was added a solution of 3-formylaminopropyn (17 g, 0.20 mol) in DMA (15 ml), and stirring was continued at room temperature overnight. The solvent was removed in vacuo and the residue was extracted with ether (300 ml). The ether was evaporated leaving an oily residue from which the title compound was isolated by distillation (120°-140° C./0.3 mmHg); 1H-NMR (CDCl3) 2.21 (s,3H), 4.35 (d,2H), 5.97 (s,1H), 7-8 (br, 1H), 8.13 (s,1H). (Compound 15).

後処理

  1. customprepared
  2. customThe solvent was removed in vacuo
  3. extractionthe residue was extracted with ether (300 ml)
  4. customThe ether was evaporated

出典と根拠

ORDレコード
ord-696d3c6fac014446b44ee9b72b32d537
出典データセット
uspto-grants-1992_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05116841

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート