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

4-(Trifluoromethyl)aniline → HCID 11301521、化合物

HRID 898823
ノート
印刷プレビュー

反応式

HRID 898823 の反応式
[F:1][C:2]([F:11])([F:10])[C:3]1[CH:9]=[CH:8][C:6]([NH2:7])=[CH:5][CH:4]=1.[C:12]([N:17]1[CH2:21][CH2:20][O:19][C:18]1=[O:22])(=[O:16])/[CH:13]=[CH:14]/[CH3:15].[Cl-].[NH4+]>C1(C)C=CC=CC=1>[F:1][C:2]([F:10])([F:11])[C:3]1[CH:9]=[CH:8][C:6]([NH:7][CH:14]([CH3:15])[CH2:13][C:12]([N:17]2[CH2:21][CH2:20][O:19][C:18]2=[O:22])=[O:16])=[CH:5][CH:4]=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 99644-(Trifluoromethyl)anilineHCID 25517Ammonium ChlorideHCID 53658453-[(E)-2-Butenoyl]-1,3-oxazolidin-2-one

生成物 1

HCID 11301521HCID 11301521、化合物収率 75.3%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

To a solution of 4-trifluoromethylaniline (193 mg, 1.2 mmol) and 3-crotonoyl-1,3-oxazolidin-2-one (155 mg, 1.0 mmol) in toluene (3 ml) in a stream of nitrogen was added Pd((R)-binap)(H2O)2(OTf)2 (26.6 mg, 0.025 mmol) and the resulting mixture was stirred at room temperature for 16 hours. After completion of the reaction, a saturated aqueous solution of ammonium chloride (10 ml) was added to the reaction mixture and the resulting mixture was extracted with ethyl acetate (10 ml). The organic layer was dried over anhydrous magnesium sulfate. The solvent was then evaporated off and the crude product obtained was purified by a silica gel column chromatography (hexane:ethyl acetate=1:1) to give the objective compound 3-(4-trifluoromethylanilino)butyryl-1,3-oxazolidin-2-one (238 mg, 75% yield). Enantiomeric excess ratio of this product was determined by a liquid chromatography using a column for separation of optical isomers (column: AD-H) to be 83% e.e.

後処理

  1. customAfter completion of the reaction
  2. extractionthe resulting mixture was extracted with ethyl acetate (10 ml)
  3. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  4. customThe solvent was then evaporated off
  5. customthe crude product obtained
  6. customwas purified by a silica gel column chromatography (hexane:ethyl acetate=1:1)

出典と根拠

ORDレコード
ord-c2539e421c084425899c51982ee7f755
出典データセット
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07351849B2

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