Allylamine → HCID 52937224, compound

HRID 1754283Notes

Reaction equation

HRID 1754283 reaction equation
Cl[CH2:2][CH:3]([OH:7])[CH2:4][CH:5]=[CH2:6].[CH2:8]([NH2:11])[CH:9]=[CH2:10]>>[CH2:8]([NH:11][CH2:2][CH:3]([OH:7])[CH2:4][CH:5]=[CH2:6])[CH:9]=[CH2:10]

Participants

3

Conditions

Temperature
90 °C

Procedure

A mixture of 1-chloropent-4-en-2-ol (23.40 g, 194.06 mmol, 1.00 Eq) and prop-2-en-1-amine (33.00 g, 578.03 mmol, 2.98 Eq) was stirred at 90° C. for 16 hr. The mixture was cooled to 25° C. and concentrated in reduced pressure at 60° C. The residue was poured into ice-water (w/w=1/1) (150 mL) and stirred for 20 min. The aqueous phase was extracted with EA. The combined organic phase was washed with saturated brine (200 mL*2), dried with anhydrous Na2SO4, filtered and concentrated in vacuum. The residue was purified by silica gel chromatography (DCM:MeOH=30/1 to 10/1) to afford 1-(allylamino)pent-4-en-2-ol (16.00 g, 113.31 mmol, 58.39% yield) as yellow oil.

Workup

  1. temperatureThe mixture was cooled to 25° C.
  2. concentrationconcentrated in reduced pressure at 60° C
  3. additionThe residue was poured into ice-water (w/w=1/1) (150 mL)
  4. stirringstirred for 20 min
  5. extractionThe aqueous phase was extracted with EA
  6. washThe combined organic phase was washed with saturated brine (200 mL*2)
  7. dry with materialdried with anhydrous Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated in vacuum
  10. customThe residue was purified by silica gel chromatography (DCM:MeOH=30/1 to 10/1)

Sources & evidence

ORD record
ord-e699667d585c4c65a9fa55a2eb260ad5
Source dataset
uspto-grants-2015_10
Patent number
US09169212B2

Reaction notes

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