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Hexane → ((10-Undecenyl)-ethoxyphosphinyl)methylphosphonic acid dimethyl ester

HRID 2354493
ノート
印刷プレビュー

反応式

HRID 2354493 の反応式
C([Li])CCC.CCCCCC.[CH3:12][O:13][P:14]([CH3:18])(=[O:17])[O:15][CH3:16].[CH2:19]([P:30](Cl)(=[O:34])[O:31][CH2:32][CH3:33])[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH:28]=[CH2:29].[Cl-].[NH4+]>O1CCCC1.C(OCC)(=O)C>[CH3:12][O:13][P:14]([CH2:18][P:30]([CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH:28]=[CH2:29])([O:31][CH2:32][CH3:33])=[O:34])(=[O:17])[O:15][CH3:16]
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

8

反応物 5

HCID 8058HexaneHCID 12958Dimethyl methylphosphonateHCID 25517Ammonium ChlorideHCID 21054114(10-Undecenyl)phosphono chloridic acid, ethyl esterHCID 178418339Butyllithium

生成物 1

HCID 21054117((10-Undecenyl)-ethoxyphosphinyl)methylphosphonic acid dimethyl ester収率 78%

試薬・触媒・溶媒 2

HCID 8028Tetrahydrofuran溶媒HCID 8857Ethyl Acetate溶媒

反応条件

温度
-50 °C

実験手順

A 2.5 M solution of n-butyllithium in hexane (9.4 mL, 23.5 mmol) was added dropwise with stirring to methylphosphonic acid dimethyl ester (2.65 g, 21.4 mmol) in 100 mL of anhydrous tetrahydrofuran at −78° C. under a nitrogen atmosphere. After 30 minutes, (10-undecenyl)phosphono chloridic acid, ethyl ester (3 g, 10.68 mmol) was added dropwise while stirring was continued. The reaction was stirred at −78° C. for 2 hours then warmed to −50° C. and stirred for an additional 2 hours. Saturated ammonium chloride was then added to neutralize the excess base and the reaction was allowed to warm to ambient temperature. The volatiles were removed by rotary evaporation to give a viscous liquid. This liquid was diluted with ethyl acetate (200 mL) and extracted twice with water (100 mL). The organic layer was collected and dried over sodium sulfate, filtered and concentrated under rotary evaporation to give a viscous liquid. The product was then placed on a high vacuum pump to remove any remaining volatiles (3.07 g, 78% yield).

後処理

  1. stirringThe reaction was stirred at −78° C. for 2 hours
  2. stirringstirred for an additional 2 hours
  3. temperatureto warm to ambient temperature
  4. customThe volatiles were removed by rotary evaporation
  5. customto give a viscous liquid
  6. extractionextracted twice with water (100 mL)
  7. customThe organic layer was collected
  8. dry with materialdried over sodium sulfate
  9. filtrationfiltered
  10. concentrationconcentrated under rotary evaporation
  11. customto give a viscous liquid
  12. customto remove any remaining volatiles (3.07 g, 78% yield)

出典と根拠

ORDレコード
ord-b6a6601c3bff46d49a9361dd549fa1da
出典データセット
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07754200B2

反応ノート

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