Diethyl Ether → [Ethoxy(4-phenylbutyl)phosphoryl]acetic acid

HRID 746065

反応式

HRID 746065 の反応式
[C:1]1([CH2:7][CH2:8][CH2:9][CH2:10][P:11]([OH:13])[OH:12])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:14](OCC)[CH3:15].C(N(CC)CC)C.C[Si](Cl)(C)C.Br[CH2:32][C:33]([OH:35])=[O:34]>C(Cl)(Cl)Cl>[CH2:14]([O:12][P:11]([CH2:32][C:33]([OH:35])=[O:34])([CH2:10][CH2:9][CH2:8][CH2:7][C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)=[O:13])[CH3:15]

参加物

7

反応条件

温度
0 °C

実験手順

To a solution of 4-phenylbutyl phosphonous acid, ethyl ether (0.5 g, 0.0022 mole) in chloroform (10 ml) was added triethylamine (0.68 ml, 0.0048 mole) and the solution was cooled in an ice bath to 0° C. Trimethyl silyl chloride (0.6 ml, 0.0048 mole) was added to the above solution dropwise, followed by bromoacetic acid (0.34 g, 0.0024 mole). The ice bath was removed and the mixture stirred at room temperature for 5 hours and poured into 10% aqueous HCl (30 ml) and crushed ice (20 g). After shaking the mixture in a separatory funnel, the chloroform layer was separated and the aqueous layer extracted with dichloromethane (2×50 ml). The combined organic phase was washed with brine, dried over anhydrous sodium sulfate and the solvents removed on a rotavap. The resulting crude thick oil was vacuum dried to get 0.61 g (97%) of title compound in the form of an oil, TLC: Silica gel, CH2Cl2 :MeOH:HOAc shows one main spot at Rf =0.37.

後処理

  1. customThe ice bath was removed
  2. additionpoured into 10% aqueous HCl (30 ml)
  3. customcrushed ice (20 g)
  4. stirringAfter shaking the mixture in a separatory funnel
  5. customthe chloroform layer was separated
  6. extractionthe aqueous layer extracted with dichloromethane (2×50 ml)
  7. washThe combined organic phase was washed with brine
  8. dry with materialdried over anhydrous sodium sulfate
  9. customthe solvents removed on a rotavap
  10. customdried

出典と根拠

ORDレコード
ord-1f460e3036be4135ae4478e6628ba798
出典データセット
uspto-grants-1986_07
特許番号
US04602092

関連ノート

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