Ethyl Dodecanoate → HCID 14883456, compound

HRID 1284315Notes

Reaction equation

HRID 1284315 reaction equation
[CH3:1][P:2](=[O:7])([O:5][CH3:6])[O:3][CH3:4].O1CCCC1.C([Li])CCC.C([O:20][C:21](=O)[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])C>C(O)(=O)C>[O:20]=[C:21]([CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])[CH2:1][P:2](=[O:7])([O:5][CH3:6])[O:3][CH3:4]

Participants

6

Procedure

84 g. of dimethyl methylphosphonate were dissolved in 400 ml. of tetrahydrofuran and cooled to -60°C. Under an atmosphere of nitrogen, n-butyllithium (prepared from 14 g. of lithium, 116 g. of n-butyl bromide and 510 ml. of diethyl ether) was added dropwise to the solution while maintaining the temperature below -50°C. and then stirred for 30 minutes. To the solution thus obtained, 38 g. of lauric acid ethyl ester in 140 ml. of tetrahydrofuran were added at below -55°C. and stirred for 16 hours. The reaction mixture was then neutralized with acetic acid, concentrated, dissolved in a small amount of water and extracted with diethyl ether. The extracts were washed with water, dried, concentrated and distilled to give 50 g. of the title compound having the following physical characteristic:

Workup

  1. temperaturewhile maintaining the temperature below -50°C.
  2. customTo the solution thus obtained
  3. stirringstirred for 16 hours
  4. concentrationconcentrated
  5. dissolutiondissolved in a small amount of water
  6. extractionextracted with diethyl ether
  7. washThe extracts were washed with water
  8. customdried
  9. concentrationconcentrated
  10. distillationdistilled
  11. customto give 50 g

Sources & evidence

ORD record
ord-85de0ff4b6ed454e954b8a7b1f9445ec
Source dataset
uspto-grants-1976_08
Patent number
US03978229

Reaction notes

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