Acetonitrile → HCID 178476840, compound

HRID 2418668Notes

Reaction equation

HRID 2418668 reaction equation
[OH:1][CH:2]([PH:4](=[O:6])[OH:5])[CH3:3].[C:7]1([CH:17]([NH2:19])[CH3:18])[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:10]=[CH:9][CH:8]=1.C(#N)C>CO>[OH:1][CH:2]([PH:4](=[O:5])[O-:6])[CH3:3].[C:7]1([CH:17]([NH3+:19])[CH3:18])[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:10]=[CH:9][CH:8]=1

Participants

5

Reactant 3

HCID 6342AcetonitrileHCID 980891-(1-Naphthyl)ethylamineHCID 178476830HCID 178476830, compound

Product 1

HCID 178476840HCID 178476840, compoundYield 38%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent2×

Procedure

Crude α-hydroxyethylphosphinic acid (57.7 g; 0.524 mol) prepared as in Example 1 was dissolved in methanol (290 ml). α-Naphthylethylamine (90.2 g; 0.575 mol) was added thereto at a temperature of not more than 50° C. while stirring. The reaction mixture was kept at a temperature of 25° to 30° C. for 30 minutes, followed by distillation of methanol to give a foamy substance. To the foamy substance, methanol (60 ml) and acetonitrile (600 ml) were added, followed by vigorous stirring, whereby crystals were precipitated. To the resultant mixture, methanol (130 ml) was added, followed by heating with reflux. After cooling, precipitated crystals were collected by filtration to give (±)-α-naphthylethylammonium α-hydroxyethylphosphinate (Compound No. 22) (56.0 g). M.P., 164° C. Yield, 37.8%. The mother liquor was concentrated, and the residue was recrystallized from a mixture of acetonitrile (400 ml) and methanol (105 ml) to give (±)-α-naphthylethylammonium α-hydroxyethylphosphinate (23.0 g). The thus prepared (±)-α-naphthylethylammonium α-hydroxyethylphosphinate (73.6 g; 0.2616 mol) was dissolved in distilled water (500 ml), cation exchange resin (Dowex 50W ×8H+ type; 600 g) was added thereto, and the resultant mixture was stirred for 40 minutes. After separation of the resin, the filtrate was concentrated to give pure α-hydroxyethylphosphinic acid (Compound No. 1) (27.0 g). Yield, 93.8%. No peak due to any impurity was recognized by NMR.

Workup

  1. distillationfollowed by distillation of methanol
  2. customto give a foamy substance
  3. customwere precipitated
  4. additionTo the resultant mixture, methanol (130 ml) was added
  5. temperatureby heating
  6. temperaturewith reflux
  7. temperatureAfter cooling
  8. customprecipitated crystals
  9. filtrationwere collected by filtration

Sources & evidence

ORD record
ord-4148ce2cb9444784b0b0b30bb39c13b1
Source dataset
uspto-grants-1984_09
Patent number
US04473561

Reaction notes

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