Trifluoroacetic acid → 2,2,2-trifluoro-N-(6-isopropoxy-3-oxo-2,3-dihydro-1H-inden-1-yl)acetamide

HRID 501734ノート

反応式

HRID 501734 の反応式
[NH2:1][CH:2]([C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([O:13][CH:14]([CH3:16])[CH3:15])[CH:8]=1)[CH2:3][C:4]([OH:6])=O.[C:17](O)([C:19]([F:22])([F:21])[F:20])=[O:18].C(OC(C(F)(F)F)=O)(C(F)(F)F)=O.CCOC(C)=O>O>[F:20][C:19]([F:22])([F:21])[C:17]([NH:1][CH:2]1[C:7]2[C:12](=[CH:11][CH:10]=[C:9]([O:13][CH:14]([CH3:16])[CH3:15])[CH:8]=2)[C:4](=[O:6])[CH2:3]1)=[O:18]

参加物

6

反応物 4

HCID 6422Trifluoroacetic acidHCID 8857Ethyl AcetateHCID 9845Trifluoroacetic anhydrideHCID 230026273-Amino-3-(3-isopropoxyphenyl)propanoic acid

生成物 1

HCID 866223552,2,2-trifluoro-N-(6-isopropoxy-3-oxo-2,3-dihydro-1H-inden-1-yl)acetamide収率 23%

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
95 °C

実験手順

Step AU (3). To a solution of 3-amino-3-(3-isopropoxyphenyl)propanoic acid (65 g, 291 mmol) and TFA (100 mL) was added TFAA (100 mL). The mixture was warmed up to 95° C. for 2 h. The solvent was evaporated under high vacuum to afford a sticky oil which was taken into EtOAc (500 mL) and water (300 mL). The organic layer was separated, dried over Na2SO4, and concentrated in vacuo. The residue was purified using silica-gel chromatography (10-30% EtOAc/Hexane) to afford 20 g (23% yield) of 2,2,2-trifluoro-N-(6-isopropoxy-3-oxo-2,3-dihydro-1H-inden-1-yl)acetamide as a white solid.

後処理

  1. customThe solvent was evaporated under high vacuum
  2. customto afford a sticky oil which
  3. customThe organic layer was separated
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated in vacuo
  6. customThe residue was purified

出典と根拠

ORDレコード
ord-f189131343fb40afa5c7fcc3f6d371d7
出典データセット
uspto-grants-2010_08
特許番号
US07772221B2

反応ノート

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