Propylamine → HCID 19917485, compound

HRID 1708672Notes

Reaction equation

HRID 1708672 reaction equation
[CH2:1]([NH2:4])[CH2:2][CH3:3].[Cl:5][CH:6]=[CH:7][CH2:8]Cl>>[ClH:5].[Cl:5]/[CH:6]=[CH:7]/[CH2:8][NH:4][CH2:1][CH2:2][CH3:3]

Participants

3

Procedure

To 19.7 ml (0.24 mol) of n-propylamine was added 1.82 ml (20 mmol) of 1,3-dichloropropene (E/Z=9/1) under ice cooling. The mixture was stirred for 3 hours at the same temperature, and concentrated under reduced pressure to remove n-propylamine. The residue was treated with 50 ml of ethyl acetate and precipitated n-propylamine hydrochloride was filtered and washed with 10 ml of ethyl acetate. The filtrate and washing were combined, washed with 20 ml of saturated sodium hydrogen carbonate aqueous solution and 20 ml of water and 20 ml of saturated sodium chloride aqueous solution, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The yellow residual oil was dissolved in 4 ml of 23% hydrogen chloride methanol solution. The solvent and excess hydrogen chloride were distilled off under reduced pressure. The resulting crystals were suspended in 8 ml of diisopropyl ether, filtered, washed with 1 ml×2 of diisopropyl ether and then dried to obtain 2.38 g (yield: 70%) of the above identified compound as slightly yellowish brown crystalline powder.

Workup

  1. concentrationconcentrated under reduced pressure
  2. customto remove n-propylamine
  3. additionThe residue was treated with 50 ml of ethyl acetate
  4. customprecipitated n-propylamine hydrochloride
  5. filtrationwas filtered
  6. washwashed with 10 ml of ethyl acetate
  7. washThe filtrate and washing
  8. washwashed with 20 ml of saturated sodium hydrogen carbonate aqueous solution and 20 ml of water and 20 ml of saturated sodium chloride aqueous solution
  9. dry with materialdried over anhydrous magnesium sulfate
  10. concentrationconcentrated under reduced pressure
  11. dissolutionThe yellow residual oil was dissolved in 4 ml of 23% hydrogen chloride methanol solution
  12. distillationThe solvent and excess hydrogen chloride were distilled off under reduced pressure
  13. filtrationfiltered
  14. washwashed with 1 ml×2 of diisopropyl ether
  15. customdried
  16. customto obtain 2.38 g (yield: 70%) of the

Sources & evidence

ORD record
ord-18de59cd4907455eb4a4d11ec0d45ee3
Source dataset
uspto-grants-1994_10
Patent number
US05359091

Reaction notes

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