Morpholine → HCID 59758720, compound
Reaction equation
[NH:1]1[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.[CH3:7][Si:8]([CH3:23])([CH2:17][CH2:18][Si:19]([CH3:22])([CH3:21])[CH3:20])[CH2:9][CH2:10][CH2:11][O:12][CH2:13][CH:14]1[CH2:16][O:15]1>C(O)C>[CH3:23][Si:8]([CH3:7])([CH2:17][CH2:18][Si:19]([CH3:20])([CH3:22])[CH3:21])[CH2:9][CH2:10][CH2:11][O:12][CH2:13][CH:14]([OH:15])[CH2:16][N:1]1[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 70 °C
Procedure
Morpholine (0.634 g; 7.28 mMol) and 40 mL of ethanol were charged to a 100 mL Rb flask equipped with a magnetic stirrer. The mixture was stirred and heated to 70° C. 2-{3-[Dimethyl-(2-trimethylsilanyl-ethyl)-silanyl]-propoxymethyl}-oxirane 8 (2 g; 7.28 mMol) mixed with 10 g ethanol was placed in an addition funnel and added dropwise to the flask. The mixture was stirred and maintained at 70° C. for an additional 4 hours. Ethanol was stripped off on the rotovap. The mixture was distilled under vacuum to remove impurities.
Workup
- customequipped with a magnetic stirrer
- customwas placed in an addition funnel
- additionadded dropwise to the flask
- stirringThe mixture was stirred
- temperaturemaintained at 70° C. for an additional 4 hours
- distillationThe mixture was distilled under vacuum
- customto remove impurities
Sources & evidence
- ORD record
- ord-f76a48f7dd304fa2830280ace3c3b6af
- Source dataset
- uspto-grants-2013_10
- Patent number
- US08569385B2
Reaction notes
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