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Methyl iodide → 8-Methoxy-8-(trifluoromethyl)-1,4-dioxaspiro[4.5]decane

HRID 922118
ノート
印刷プレビュー

反応式

HRID 922118 の反応式
[F:1][C:2]([F:15])([F:14])[C:3]1([OH:13])[CH2:12][CH2:11][C:6]2([O:10][CH2:9][CH2:8][O:7]2)[CH2:5][CH2:4]1.[H-].[Na+].I[CH3:19]>O1CCCC1>[CH3:19][O:13][C:3]1([C:2]([F:1])([F:14])[F:15])[CH2:4][CH2:5][C:6]2([O:7][CH2:8][CH2:9][O:10]2)[CH2:11][CH2:12]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 6328Methyl iodideHCID 24758Sodium hydrideHCID 616452568-(Trifluoromethyl)-1,4-dioxaspiro[4.5]decan-8-ol

生成物 1

HCID 712468178-Methoxy-8-(trifluoromethyl)-1,4-dioxaspiro[4.5]decane

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

At 0° C., 16.23 g (71.75 mmol) of 8-(trifluoromethyl)-1,4-dioxaspiro[4.5]decan-8-ol (Example 7A) were dissolved in 582 ml of tetrahydrofuran, 5.74 g (143.50 mmol) of sodium hydride (60% in paraffin oil) were added a little at a time and the mixture was stirred at room temperature for 1 hour. 50.92 g (358.76 mmol) of iodomethane were added dropwise to the resulting suspension, and the reaction mixture was stirred at room temperature overnight. For work-up, the mixture was poured into about 1 l of ice-water and the product was extracted with dichloromethane. The organic phase was washed repeatedly with water, dried over sodium sulphate and concentrated under reduced pressure. Drying gave 17.34 g (100% of theory) of the title compound as a brownish oil.

後処理

  1. stirringthe reaction mixture was stirred at room temperature overnight
  2. extractionthe product was extracted with dichloromethane
  3. washThe organic phase was washed repeatedly with water
  4. dry with materialdried over sodium sulphate
  5. concentrationconcentrated under reduced pressure
  6. customDrying

出典と根拠

ORDレコード
ord-95199e1828cd4fafbdd528bb80aaa5c2
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09278925B2

反応ノート

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