1,3-Propanediamine → HCID 59001677, compound

Temperature

25 °C

To a 500 mL, three-necked round bottom flask (fitted with a reflux condenser, addition funnel, and stir bar) was added 10-undecenoyl chloride (32.2 mL, 30.4 g, 0.150 mol) and THF (200 mL). To the addition funnel was added 1,3-diaminopropane (5.56 g, 0.075 mol), triethylamine (42 mL, 30.5 g, 0.300 mol), and THF (75 mL). The amine solution was added dropwise to the acid chloride solution over one hour, yielding a white precipitate. On completion of addition, the reaction mixture was stirred at 25° C. for one hour. The reaction mixture was filtered to remove precipitated solids. The precipitated solids were added to water (250 mL) and stirred. The insoluble solid was collected via filtration, then air dried. The crude product was recrystallized from hot toluene (250 mL) to produce a white solid which was dried in vacuo at 25° C. for 16 hours. The thus obtained compound is represented by formula (10) shown below. Yield: 9.6 g (31%). M.P.: 117° C. to 119° C. 1H and 13C NMR analyses were consistent with the structure of formula (10).

1. customTo a 500 mL, three-necked round bottom flask (fitted with a reflux condenser, addition funnel, and stir bar)
2. customyielding a white precipitate
3. additionOn completion of addition
4. filtrationThe reaction mixture was filtered
5. customto remove
6. customprecipitated solids
7. additionThe precipitated solids were added to water (250 mL)
8. stirringstirred
9. filtrationThe insoluble solid was collected via filtration
10. customair dried
11. customThe crude product was recrystallized from hot toluene (250 mL)
12. customto produce a white solid which
13. customwas dried in vacuo at 25° C. for 16 hours

ORD record

ord-dd5f2a3e64fd49148445f7d493fa1a4e

Source dataset

uspto-grants-2007_11

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07300986B2