反応 #345235

ord-b6eed6d57842473bba9297d866dea750

反応方程式

C=C(C)C(=O)Cl
methacryloyl chloride
O=C1CCCCCN1
caprolactam
O=C1CCCCCN1
ε-caprolactam
[Na]
sodium
[Na]
sodium
C=C(C)C(=O)N1CCCCCC1=O
N-Methacryloylcaprolactam

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONThe mixture is then poured into a separatory funnel
  2. 2
    洗浄washed with 200 ml water, 200 ml of sodium dicarbonate solution
  3. 3
    抽出The organic compounds are extracted with ether from the water phase
  4. 4
    乾燥the ether solution and benzene solution are dried over CaCl2
  5. 5
    その他the solvent evaporated under reduced pressure
  6. 6
    その他comes off at 90° C.

実験手順

74 g of ε-caprolactam in 700 ml dry toluene is heated with 9.5 g of sodium at 90°-95° C. When all of the sodium metal has reacted, 43 ml of methacryloyl chloride in 50 ml dry benzene is added dropwise into the voluminous caprolactam salts at 4°-6° C. The mixture is then poured into a separatory funnel, washed with 200 ml water, 200 ml of sodium dicarbonate solution, and again with 20 ml water. The organic compounds are extracted with ether from the water phase, and the ether solution and benzene solution are dried over CaCl2 and the solvent evaporated under reduced pressure. The product, N-methacryloylcaprolactam, comes off at 90° C./2 mm hg. The yield is 32.3 g (42.8% based on sodium).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05264491uspto-grants-1993_11