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Trifluoroacetic acid → 2-(4-Methoxyphenyl)-6-methoxy-1-tetralone

HRID 617910
ノート
印刷プレビュー

反応式

HRID 617910 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH:9]([CH2:13][CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([O:21][CH3:22])[CH:16]=2)[C:10]([OH:12])=O)=[CH:5][CH:4]=1.FC(F)(F)C(O)=O>C(Cl)Cl>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([CH:9]2[CH2:13][CH2:14][C:15]3[C:20](=[CH:19][CH:18]=[C:17]([O:21][CH3:22])[CH:16]=3)[C:10]2=[O:12])=[CH:7][CH:8]=1
参加物反応条件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 6422Trifluoroacetic acidHCID 215844042-(4-Methoxyphenyl)-4-(3-methoxyphenyl)butyric acid

生成物 1

HCID 134065432-(4-Methoxyphenyl)-6-methoxy-1-tetralone

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
0 °C

実験手順

2.31 g (7.7 mmol) of 2-(4-methoxyphenyl)-4-(3-Methoxyphenyl)butyric acid was dissolved in 30 mL of CH2Cl2 and cooled to 0° C. To this solution was added 3.4 ml (23.1 mmol) of trifluoroacetic acid, the reaction was allowed to proceed for 30 minutes. The reaction was quenched by pouring into an aqueous solution of NaHCO3. The organic layer was separated, washed twice with NaHCO3 solution washed twice with brine, dried with Na2SO4, and evaporated to a solid. This yielded 1.5 g of the title compound as a tan amorphous solid.

後処理

  1. customThe reaction was quenched
  2. additionby pouring into an aqueous solution of NaHCO3
  3. customThe organic layer was separated
  4. washwashed twice with NaHCO3 solution
  5. washwashed twice with brine
  6. dry with materialdried with Na2SO4
  7. customevaporated to a solid

出典と根拠

ORDレコード
ord-f2245fd701e34dac8ae1db1bb6ef7537
出典データセット
uspto-grants-1999_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05952350

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート