Diethanolamine → HCID 59000137, compound
Reaction equation
[CH2:1]([CH:3]([CH2:10][CH2:11][CH2:12][CH3:13])[CH2:4][O:5][CH2:6][CH:7]1[O:9][CH2:8]1)[CH3:2].[NH:14]([CH2:18][CH2:19][OH:20])[CH2:15][CH2:16][OH:17].C(OCC1OC1)C1OC1>>[OH:17][CH2:16][CH2:15][N:14]([CH2:18][CH2:19][OH:20])[CH2:8][CH:7]([OH:9])[CH2:6][O:5][CH2:4][CH:3]([CH2:1][CH3:2])[CH2:10][CH2:11][CH2:12][CH3:13]Participants
4
Conditions
- Temperature
- 77.5 °C
Procedure
A three-necked, septum capped, 250 mL, round-bottom flask equipped with an addition funnel and containing a magnetic stirring bar is flushed with argon and charged with 2-ethylhexylglycidyl ether (66.53 g, 0.35 mol). Diethanolamine (40.89 g, 0.38 mol) is added during 10 min to the glycidyl ether, with stirring. The flask is placed in an oil bath and heated at a bath temperature of 75-80° C. overnight. The reaction is cooled and checked by 1H NMR to ensure the complete consumption of the glycidyl ether. A colorless viscous liquid is obtained.
Workup
- customA three-necked, septum capped
- custom250 mL, round-bottom flask equipped with an addition funnel
- additioncontaining a magnetic stirring bar
- customis flushed with argon
- customThe flask is placed in an oil bath
- temperatureThe reaction is cooled
- customthe complete consumption of the glycidyl ether
- customA colorless viscous liquid is obtained
Sources & evidence
- ORD record
- ord-a00a63a051a2468798f0be96db48ff92
- Source dataset
- uspto-grants-2008_01
- Patent number
- US07318843B2
Reaction notes
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