Acetate → Dimethyl [2-oxo-3-(thiophen-2-yl)propyl]phosphonate

HRID 614041Notes

Reaction equation

HRID 614041 reaction equation
C([O-])(=O)C.[CH3:5][P:6](=[O:11])([O:9][CH3:10])[O:7][CH3:8].P(=O)([O-])[O-].C([Li])CCC.[S:21]1[CH:25]=[CH:24][CH:23]=[C:22]1[CH2:26][C:27](OC)=[O:28]>O1CCCC1.CCCCCC.C(O)(=O)C>[O:28]=[C:27]([CH2:26][C:22]1[S:21][CH:25]=[CH:24][CH:23]=1)[CH2:5][P:6](=[O:11])([O:9][CH3:10])[O:7][CH3:8]

Participants

9

Reactant 5

HCID 175AcetateHCID 406CID 406HCID 12958Dimethyl methylphosphonateHCID 88055Methyl thiophen-2-acetateHCID 178418339Butyllithium

Product 1

HCID 21329763Dimethyl [2-oxo-3-(thiophen-2-yl)propyl]phosphonate

Reagents, catalysts & solvents 3

HCID 176Acetic AcidSolventHCID 8028TetrahydrofuranSolventHCID 8058HexaneSolvent

Procedure

A solution of 37.2 g (0.3 -thienyl)acetate mole) dimethyl methylphosphonate (Aldrich) in 400 ml dry tetrahydrofuran was cooled to -78° in a dry nitrogen atmosphere. To the stirred phosphonate solution was added 194 ml of 1.6 M n-butyllithium in hexane solution (Alfa Inorganics, Inc.) dropwise over a period of 18 minutes at such a rate that the reaction temperature never rose above -65°. After an additional 5 minutes stirring at -78°, 23.4 g (0.15 mole) methyl 2-(2 -thienyl)acetate was added dropwise at a rate that kept the reaction temperature less than -70° (20 minutes). After 3.5 hours at -78° the reaction mixture was allowed to warm to ambient temperature, neutralized with 6 ml acetic acid and rotary evaporated to a white gel. The gelatinous material was taken up in 75 ml water the aqueous phase extracted with 100 ml portions of chloroform (3a) the combined organic extracts were backwashed (50 ml H2O), dried (MgSO4), and concentrated (water aspirator) to a crude residue and distilled, b.p. 150-52° (<0.5 mm) to give 4.8 g dimethyl 2-oxo-3-(2-thienyl)propylphosphonate (2a).

Workup

  1. customthe reaction temperature less than -70° (20 minutes)
  2. waitAfter 3.5 hours at -78° the reaction mixture was allowed
  3. customrotary evaporated to a white gel
  4. extractionextracted with 100 ml portions of chloroform (3a) the combined organic extracts
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated (water aspirator) to a crude residue
  7. distillationdistilled

Sources & evidence

ORD record
ord-ad0fa5f4896c44b78ff6607a3df0bcce
Source dataset
uspto-grants-1979_03
Patent number
US04143051

Reaction notes

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