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tert-Butyl hydroperoxide → 4-(trifluoromethyl)-6,6a-dihydro-1aH-indeno[1,2-b]oxirene

HRID 2178770
ノート
印刷プレビュー

反応式

HRID 2178770 の反応式
[F:1][C:2]([F:13])([F:12])[C:3]1[CH:11]=[C:10]2[C:6]([CH:7]=[CH:8][CH2:9]2)=[CH:5][CH:4]=1.C([O:18]O)(C)(C)C>ClCCl.CCCCCCCCCC.[Ti](Cl)(Cl)(Cl)Cl>[F:1][C:2]([F:12])([F:13])[C:3]1[CH:4]=[CH:5][C:6]2[CH:7]3[O:18][CH:8]3[CH2:9][C:10]=2[CH:11]=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

6

反応物 2

HCID 6410tert-Butyl hydroperoxideHCID 190955106-(trifluoromethyl)-1H-indene

生成物 1

HCID 592126284-(trifluoromethyl)-6,6a-dihydro-1aH-indeno[1,2-b]oxirene

試薬・触媒・溶媒 3

HCID 24193Titanium Tetrachloride触媒HCID 6344Dichloromethane溶媒HCID 15600Decane溶媒

反応条件

温度
-78 °C

実験手順

To a solution of 6-(trifluoromethyl)-1H-indene (1.1 g, 6 mmol) in anhydrous dichloromethane (80 mL) at −78° C. was added a 5.5 M solution of tert-butyl hydroperoxide in n-decane (1.3 mL) followed by titanium tetrachloride (0.79 mL, 7.2 mmol). After being stirred at −78° C. for 1 h, the resulting brown solution was quenched with a mixture of Et2O/saturated Na2SO3 solution. The mixture was stirred at ambient temperature for 1 h to give a colorless solution. The organic layer was separated and washed with brine, dried over MgSO4 and concentrated to give the crude product (1.2 g) as a solid. LC/MS calculated for C10H2F3O: (M+H)+201; found 201.0.

後処理

  1. customthe resulting brown solution was quenched with a mixture of Et2O/saturated Na2SO3 solution
  2. stirringThe mixture was stirred at ambient temperature for 1 h
  3. customto give a colorless solution
  4. customThe organic layer was separated
  5. washwashed with brine
  6. dry with materialdried over MgSO4
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-9cf0a8f8506b4b01b5e8a8897360f1cc
出典データセット
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09067921B2

反応ノート

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