Acetic Acid → Dimethyl 4-(3-trifluoromethylphenyl)-2-oxobutylphosphonate

HRID 1389177Notes

Reaction equation

HRID 1389177 reaction equation
C([Li])CCC.[CH3:6][P:7](=[O:12])([O:10][CH3:11])[O:8][CH3:9].[F:13][C:14]([F:29])([F:28])[C:15]1[CH:16]=[C:17]([CH2:21][CH2:22][C:23](OCC)=[O:24])[CH:18]=[CH:19][CH:20]=1.C(O)(=O)C>CCCCCC.C(OCC)C.O1CCCC1>[F:13][C:14]([F:28])([F:29])[C:15]1[CH:16]=[C:17]([CH2:21][CH2:22][C:23](=[O:24])[CH2:6][P:7](=[O:12])([O:10][CH3:11])[O:8][CH3:9])[CH:18]=[CH:19][CH:20]=1

Participants

8

Conditions

Temperature
-60 °C

Procedure

A solution of n-butyl lithium (5.88 g) in hexane (48 ml) and anhydrous diethyl ether (70 ml) was added to a stirred solution of dimethyl methylphosphonate (11.4 g) in anhydrous tetrahydrofuran (50 ml) at -50° C. in an atmosphere of nitrogen during 20 minutes. The solution was stirred for a further 15 minutes at -60° C., and was then treated with a solution of ethyl 3-(3-trifluoromethylphenyl)-propionate (11.3 g) in anhydrous tetrahydrofuran (20 ml) during 10 minutes at -60° C. The solution was stirred at -60° C. for 90 minutes and then at ambient temperature for 2 hours. The solution was then treated with acetic acid (10 ml) and the solvents were evaporated off under reduced pressure. Water (75 ml) was added to the resulting gelatinous residue and the mixture was extracted with diethyl ether. The ethereal solution was washed with water, with aqueous sodium bicarbonate solution (10% w/v), and with water, dried over magnesium sulphate, and evaporated. The residue was distilled to give dimethyl 4-(3-trifluoromethylphenyl)-2-oxobutylphosphonate (7.4 g) in the form of a colourless oil, b.p. 157°-159° C./0.2 mm Hg. [elemental analysis: C, 48.3; H, 5.1; P, 9.8%. C13H16F3O4P requires C, 48.15; H, 5.0; P, 9.55%. νmax 1035, 1125, 1165, 1265, 1330, 1555 and 1720 cm-1 ].

Workup

  1. stirringThe solution was stirred at -60° C. for 90 minutes
  2. waitat ambient temperature for 2 hours
  3. customthe solvents were evaporated off under reduced pressure
  4. additionWater (75 ml) was added to the resulting gelatinous residue
  5. extractionthe mixture was extracted with diethyl ether
  6. washThe ethereal solution was washed with water, with aqueous sodium bicarbonate solution (10% w/v)
  7. dry with materialwith water, dried over magnesium sulphate
  8. customevaporated
  9. distillationThe residue was distilled

Sources & evidence

ORD record
ord-86299ac5570241b799b46c7f799e1d6d
Source dataset
uspto-grants-1981_01
Patent number
US04243683

Reaction notes

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