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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
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Water → 6-Benzoxazolol, 2-(trifluoromethyl)-

HRID 1271824
ノート
印刷プレビュー

反応式

HRID 1271824 の反応式
O[C:2]1[CH:7]=[C:6]([OH:8])[CH:5]=[CH:4][C:3]=1[NH:9][C:10](=[O:15])[C:11]([F:14])([F:13])[F:12].C1(C)C=CC(S(O)(=O)=O)=CC=1.O>C1(C)C=CC=CC=1>[F:14][C:11]([F:12])([F:13])[C:10]1[O:15][C:2]2[CH:7]=[C:6]([OH:8])[CH:5]=[CH:4][C:3]=2[N:9]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 6101p-Toluenesulfonic acidHCID 18454996N-(2,4-dihydroxyphenyl)-2,2,2-trifluoro-acetamide

生成物 1

HCID 184549866-Benzoxazolol, 2-(trifluoromethyl)-収率 40.8%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

A stirred solution of 0.8 gram (0.0036) of N-(2,4-dihydroxyphenyl)-2,2,2-trifluoroacetamide and a catalytic amount of p-toluenesulfonic acid in 50 mL of toluene was heated at reflux during an 18 hour period while the theoretical amount of water by-product was collected in a Dean-Stark trap. After this time the reaction mixture was concentrated under reduced pressure to a residue. The residue was purified with column chromatography on silica gel using methylene chloride as an eluant. The appropriate fractions were combined and concentrated under reduced pressure, yielding 0.3 gram of the subject compound. The NMR spectrum was consistent with the proposed structure.

後処理

  1. customwas collected in a Dean-Stark trap
  2. concentrationAfter this time the reaction mixture was concentrated under reduced pressure to a residue
  3. customThe residue was purified with column chromatography on silica gel
  4. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-e8b1e945ae2243caabc427497c88209b
出典データセット
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07208450B2

反応ノート

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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