HCID 86746127, compound → HCID 86746126, compound

HRID 1885472Notes

Reaction equation

HRID 1885472 reaction equation
[P:1](=[O:42])([O:36][CH2:37][CH2:38][CH2:39][CH2:40][CH3:41])([O:34][CH3:35])[O:2][CH:3]([CH2:11][O:12]C(C1C=CC(OC)=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[CH2:4][O:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]>C(Cl)(Cl)Cl.CO>[P:1](=[O:42])([O:36][CH2:37][CH2:38][CH2:39][CH2:40][CH3:41])([O:34][CH3:35])[O:2][CH:3]([CH2:11][OH:12])[CH2:4][O:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]

Participants

4

Procedure

To a solution of 13.5 g of phosphoric acid, 1-[[(4-methoxyphenyl)diphenylmethoxy]-methyl]-2-(pentyloxy)ethyl methyl pentyl ester in 68 ml of chloroform and 136 ml of methyl alcohol heated to boiling is slowly added 6.8 g of Amberlyst®-15 resin. The heat is removed and the mixture stirred at ambient temperature for 2 hours. The volatiles are removed and the residue dissolved in chloroform then washed with dilute sodium bicarbonate, dried and evaporated to an oily residue which is purified on silica gel using 1:1 ethyl acetate:hexanes to give 6 g of the desired compound as a colorless oil.

Workup

  1. customThe heat is removed
  2. customThe volatiles are removed
  3. dissolutionthe residue dissolved in chloroform
  4. washthen washed with dilute sodium bicarbonate
  5. customdried
  6. customevaporated to an oily residue which
  7. customis purified on silica gel using 1:1 ethyl acetate

Sources & evidence

ORD record
ord-39801878069548c195db525d4ce520d3
Source dataset
uspto-grants-1992_09
Patent number
US05144045

Reaction notes

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