Methyl Acrylate → HCID 131734482, compound

HRID 590533Notes

Reaction equation

HRID 590533 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

  1. customA flask equipped with a stirrer
  2. temperaturereflux condenser
  3. distillationOn distillation of the reaction solution, 219.9 g of a fraction
  4. customwas collected

Sources & evidence

ORD record
ord-61dd056323314b5291c3f737c6851283
Source dataset
uspto-grants-2016_01
Patent number
US09233988B2

Reaction notes

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