Methyl Acrylate → HCID 131734482, compound
Reaction equation
[Si:1]([N:8]1[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]1)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].[C:14]([O:18][CH3:19])(=[O:17])[CH:15]=[CH2:16]>>[Si:1]([N:8]1[CH2:13][CH2:12][N:11]([CH2:16][CH2:15][C:14]([O:18][CH3:19])=[O:17])[CH2:10][CH2:9]1)([C:4]([CH3:7])([CH3:5])[CH3:6])([CH3:3])[CH3:2]Participants
3
Conditions
- Temperature
- 70 °C
Procedure
A flask equipped with a stirrer, reflux condenser, dropping funnel and thermometer was charged with 160.3 g (0.8 mol) of 1-t-butyldimethylsilylpiperazine (Synthesis Example 1) and heated at 70° C. Once the internal temperature became steady, 75.8 g (0.88 mol) of methyl acrylate was added dropwise over 2 hours. Stirring was continued for 4 hours at the temperature. On distillation of the reaction solution, 219.9 g of a fraction having a boiling point of 135-137° C./0.4 kPa was collected.
Workup
- customA flask equipped with a stirrer
- temperaturereflux condenser
- distillationOn distillation of the reaction solution, 219.9 g of a fraction
- customwas collected
Sources & evidence
- ORD record
- ord-61dd056323314b5291c3f737c6851283
- Source dataset
- uspto-grants-2016_01
- Patent number
- US09233988B2
Reaction notes
Loading…