Allylamine → HCID 52937224, compound
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
- temperatureThe mixture was cooled to 25° C.
- concentrationconcentrated in reduced pressure at 60° C
- additionThe residue was poured into ice-water (w/w=1/1) (150 mL)
- stirringstirred for 20 min
- extractionThe aqueous phase was extracted with EA
- washThe combined organic phase was washed with saturated brine (200 mL*2)
- dry with materialdried with anhydrous Na2SO4
- filtrationfiltered
- concentrationconcentrated in vacuum
- 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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