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

Stannous Chloride → 2-Amino-5-(trifluoromethyl)phenol

HRID 612626
ノート
印刷プレビュー

反応式

HRID 612626 の反応式
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]([F:13])([F:12])[F:11])=[CH:6][C:5]=1[OH:14])([O-])=O.Cl[Sn]Cl>CCO>[NH2:1][C:4]1[CH:9]=[CH:8][C:7]([C:10]([F:11])([F:12])[F:13])=[CH:6][C:5]=1[OH:14]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24479Stannous ChlorideHCID 140916902-Nitro-5-(trifluoromethyl)phenol

生成物 1

HCID 155242772-Amino-5-(trifluoromethyl)phenol

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

2-Amino-5-trifluoromethylphenol was prepared by treating 2-nitro-5-trifluoromethylphenol (500 mg, 2.41 mmol) with a solution of SnCl2 (3.5 g, mmol) in EtOH at 23° C. for 12 h. The mixture was concentrated to 50 mL and adjusted to pH 7 using saturated sodium bicarbonate. The reaction mixture was partitioned between H2O and EtOAc. The aqueous layer was separated and extracted with EtOAc. The combined organic extracts were dried over sodium sulfate, filtered and concentrated in vacuo. The resulting colorless oil (370 mg, 87%) was used without further purification. 1H NMR (CDCl3); 7.6 (s, 1H), 7.39 (d, 1H, J=8.5 Hz), 7.08 (d, 1H, J=8.5 Hz)

後処理

  1. concentrationThe mixture was concentrated to 50 mL
  2. customThe reaction mixture was partitioned between H2O and EtOAc
  3. customThe aqueous layer was separated
  4. extractionextracted with EtOAc
  5. dry with materialThe combined organic extracts were dried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe resulting colorless oil (370 mg, 87%) was used without further purification

出典と根拠

ORDレコード
ord-eac29e9713904d379542def69d024258
出典データセット
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06005008

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