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

Sodium Hydroxide → Benzaldehyde, 2-(trifluoromethoxy)-, oxime

HRID 1748149
ノート
印刷プレビュー

反応式

HRID 1748149 の反応式
[OH-:1].[Na+].[NH2:3]O.Cl.[F:6][C:7]([F:18])([F:17])[O:8][C:9]1[CH:16]=[CH:15][CH:14]=[CH:13][C:10]=1[CH:11]=O>O.C(O)C>[F:6][C:7]([F:18])([F:17])[O:8][C:9]1[CH:16]=[CH:15][CH:14]=[CH:13][C:10]=1/[CH:11]=[N:3]/[OH: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 14798Sodium HydroxideHCID 443297Hydroxyamine hydrochlorideHCID 27771922-(Trifluoromethoxy)benzaldehyde

生成物 1

HCID 58138479Benzaldehyde, 2-(trifluoromethoxy)-, oxime

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962Water溶媒3 回

実験手順

To a solution of sodium hydroxide (7 g, 175.00 mmol, 1.19 equiv) in water (120 mL) was added a stirred solution of NH2OH.HCl (11.8 g, 169.78 mmol, 1.15 equiv) in water (120 mL) at 0°C. The resulting solution was stirred fo(10 min at 0°C. Then a solution of 2-(trifluoromethoxy)benzaldehyde (28 g, 147.29 mmol, 1.00 equiv) in ethanol (120 mL) was added. The resulting solution was allowed to stir for an additional 1 h at room temperature. The resulting solution was diluted with 500 ml of H2O, extracted with 2×700 mL of ethyl acetate and the organic layers were combined, washed with 2×300 mL of brine, dried over anhydrous sodium sulfate and concentrated under vacuum to give (E)-2-(trifluoromethoxy)benzaldehyde oxime as an off-white crystalline solid.

後処理

  1. custom10 min
  2. customat 0°C
  3. stirringto stir for an additional 1 h at room temperature
  4. extractionextracted with 2×700 mL of ethyl acetate
  5. washwashed with 2×300 mL of brine
  6. dry with materialdried over anhydrous sodium sulfate
  7. concentrationconcentrated under vacuum

出典と根拠

ORDレコード
ord-8a9155f18df84d49b08717ca4f761ba2
出典データセット
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09150568B2

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