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

Sulfuric Acid → 2,2-bisfluoromethyl-6-nitro-2H-1-benzopyran-4-carboamide

HRID 1601414
ノート
印刷プレビュー

反応式

HRID 1601414 の反応式
[C:1]([C:3]1[C:8]2[CH:9]=[C:10]([N+:13]([O-:15])=[O:14])[CH:11]=[CH:12][C:7]=2[O:6][C:5]([CH2:18][F:19])([CH2:16][F:17])[CH:4]=1)#[N:2].S(=O)(=O)(O)[OH:21]>>[F:19][CH2:18][C:5]1([CH2:16][F:17])[CH:4]=[C:3]([C:1]([NH2:2])=[O:21])[C:8]2[CH:9]=[C:10]([N+:13]([O-:15])=[O:14])[CH:11]=[CH:12][C:7]=2[O:6]1
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 1118Sulfuric AcidHCID 211949804-cyano-2,2-bisfluoromethyl-6-nitro-2H-1-benzopyran

生成物 1

HCID 218313032,2-bisfluoromethyl-6-nitro-2H-1-benzopyran-4-carboamide

実験手順

A mixture of 3 g of 4-cyano-2,2-bisfluoromethyl-6-nitro-2H-1-benzopyran and 20 ml of sulfuric acid was stirred for 36 hours. The reaction mixture was poured into ice water and the separated crystal was collected by filtration. The above-obtained crystal was diluted with ethyl acetate and the organic layer was washed with water and dried. The solvent was distilled off to obtain 3 g of 2,2-bisfluoromethyl-6-nitro-2H-1-benzopyran-4-carboamide represented by the following formula.

後処理

  1. filtrationthe separated crystal was collected by filtration
  2. additionThe above-obtained crystal was diluted with ethyl acetate
  3. washthe organic layer was washed with water
  • customdried
  • distillationThe solvent was distilled off
  • 出典と根拠

    ORDレコード
    ord-9dcc09aabe2d4e90bb70ee11eb734af6
    出典データセット
    uspto-grants-1999_11
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US05977167

    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