Acetone → HCID 22609181, compound
Reaction equation
[NH:1]([CH2:5][CH2:6][OH:7])[CH2:2][CH2:3][OH:4].[CH3:8][C:9]([CH3:11])=O.C(=O)([O-])[O-].[K+].[K+]>>[CH3:8][C:9]1([CH3:11])[N:1]([CH2:5][CH2:6][OH:7])[CH2:2][CH2:3][O:4]1Participants
Procedure
To a 100 mL flask containing diethanolamine (19.2 mL, 200 mmol) was added acetone (29.4 mL, 400 mmol, 2 eq.) and potassium carbonate (pulverised and dried at 160° C., 27.6 g, 200 mmol, 1 eq.). The reaction was stirred at room temperature for one day. The mixture was filtered through a sinter funnel (no. 3) and the collected solid was washed with acetone. The filtrate and the washes were combined and the solvent evaporated. The 1H NMR indicated a conversion of 85%. Distillation at 125-132° C./20 mmHg of the crude reaction gave the title product (20.89 g, 72% yield) as a colourless oil. 1H NMR (CDCl3, 400 MHz) d?(ppm): 3.93 (t, J=6.6 Hz, 2H); 3.62 (t, J=5.3 Hz, 2H); 2.96 (t, J=6.6 Hz, 2H); 2.65 (t, J=5.3 Hz, 2H); 1.23 (s, 6H). 13C NMR (CDCl3, 129.9 MHz) d??(ppm): 94.2; 63.5; 59.3; 50.8; 49.1; 23.3 (2C).
Workup
- filtrationThe mixture was filtered through a sinter funnel (no
- wash3) and the collected solid was washed with acetone
- customthe solvent evaporated
- distillationDistillation at 125-132° C./20 mmHg of the crude
- customreaction
Sources & evidence
- ORD record
- ord-3913289e47d64ce9938268bf8557c457
- Source dataset
- uspto-grants-2011_02
- Patent number
- US07893258B2
Reaction notes
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