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

Ethyl Acrylate → 2-((E)-2-Ethoxycarbonylvinyl)-4-trifluoromethylbenzoic Acid

HRID 491923
ノート
印刷プレビュー

反応式

HRID 491923 の反応式
N([O-])=O.[Na+].N[C:6]1[CH:14]=[C:13]([C:15]([F:18])([F:17])[F:16])[CH:12]=[CH:11][C:7]=1[C:8]([OH:10])=[O:9].[H+].[B-](F)(F)(F)F.[C:25]([O:29][CH2:30][CH3:31])(=[O:28])[CH:26]=[CH2:27]>O.C(O)C>[CH2:30]([O:29][C:25](/[CH:26]=[CH:27]/[C:6]1[CH:14]=[C:13]([C:15]([F:18])([F:17])[F:16])[CH:12]=[CH:11][C:7]=1[C:8]([OH:10])=[O:9])=[O:28])[CH3:31]
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

7

反応物 4

HCID 8821Ethyl AcrylateHCID 28118Tetrafluoroboric acid2 回HCID 678694-(Trifluoromethyl)anthranilic acidHCID 23668193Sodium Nitrite

生成物 1

HCID 576789502-((E)-2-Ethoxycarbonylvinyl)-4-trifluoromethylbenzoic Acid

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒
2 回
HCID 962Water溶媒

反応条件

温度
0 °C

実験手順

520 mg of NaNO2 (7.6 mmol) were dissolved in 2 ml of water and added dropwise at 0° C. to a solution of 1.3 g of 2-amino-4-trifluoromethylbenzoic acid (6.5 mmol) in 2.6 ml of a 48% aqueous HBF4 solution and 30 ml of ethanol. The mixture was then stirred at 0° C. for 10 minutes, then warmed to RT. A further 0.3 ml of a 48% aqueous HBF4 solution was then added, then 30 ml of ethanol, 0.9 g of ethyl acrylate (9.0 mmol) and 26.9 mg of Pd (OAc)2 (0.12 mmol). Subsequently, the mixture was stirred at 50-60° C. for 1 h. The solvent was then removed under reduced pressure, and the residue taken up with 25 ml of EA and washed initially with 25 ml of a 1N aqueous HCl solution then with 25 ml of a saturated aqueous NaCl solution. The organic phase was dried over Na2SO4 and the solvent removed under reduced pressure. The residue was suspended in 25 ml of heptane and the precipitated product was filtered off. Yield: 1.3 g (69%) of a pale brownish solid. An analytical sample was purified by crystallization from heptane/ethyl acetate.

後処理

  1. temperaturewarmed to RT
  2. stirringSubsequently, the mixture was stirred at 50-60° C. for 1 h
  3. customThe solvent was then removed under reduced pressure
  4. washwashed initially with 25 ml of a 1N aqueous HCl solution
  5. dry with materialThe organic phase was dried over Na2SO4
  6. customthe solvent removed under reduced pressure
  7. filtrationthe precipitated product was filtered off
  8. customAn analytical sample was purified by crystallization from heptane/ethyl acetate

出典と根拠

ORDレコード
ord-9a1b7bae8fe943b5994c48b4d5bac9b7
出典データセット
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07531569B2

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