반응 #985246

ord-1f1bb58ce2004b879c4d56d5e63d6e17

반응 방정식

C1CCOC1
tetrahydrofuran
CCCC[N+](CCCC)(CCCC)CCCC.O=C([O-])c1cccc(Cl)c1
tetrabutylammonium m-chlorobenzoate
CO
methanol
C1CCOC1
Tetrahydrofuran
CC(C)=C(O[Si](C)(C)C)O[Si](C)(C)C
1,1-bis(trimethylsiloxy) 2-methyl propene
CCCC[N+](CCCC)(CCCC)CCCC.O=C([O-])c1cccc(Cl)c1
tetrabutylammonium m-chlorobenzoate
C=C(C)C(=O)OCCO
2-hydroxyethyl methacrylate
C=C(C)C(=O)O
methacrylic acid
C=C(C)C(=O)OCc1ccccc1
benzyl methacrylate
C=C(C)C(=O)O.CCC(O)COCCOCCO
ethyltriethyleneglycol methacrylate

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타A 3-liter flask was equipped with a mechanical stirrer
  2. 2
    기타were started at time 0 minutes
  3. 3
    workup.ADDITIONFeed I was added over 200 minutes
  4. 4
    온도The pot was heated
  5. 5
    온도to reflux
  6. 6
    workup.DISTILLATION500 g were distilled
  7. 7
    workup.ADDITIONA solution of water (124 g) and dichloroacetic acid (0.2 g) were added to the pot and
  8. 8
    온도refluxed for 60 minutes
  9. 9
    온도After refluxing
  10. 10
    workup.DISTILLATION725 g were distilled
  11. 11
    workup.ADDITION2-pyrrolidinone (889 g) was added

실험 절차

A 3-liter flask was equipped with a mechanical stirrer, thermocouple, N2 inlet, condenser, drop funnel and syringe pump. Tetrahydrofuran (950 g), 1,1-bis(trimethylsiloxy) 2-methyl propene (46.2 g) and tetrabutylammonium m-chlorobenzoate (2 g) was added into pot. Feed I (tetrahydrofuran (5 g) and tetrabutylammonium m-chlorobenzoate (0.8 g)) and Feed II (benzyl methacrylate (600 g), 2-(trimethylsiloxy)ethyl methacrylate (312 g), ethyltriethyleneglycol methacrylate (100 g) and trimethylsilyl methacrylate (152 g)) were started at time 0 minutes. Feed I was added over 200 minutes. Feed II was added over 60 minutes. After 360 minutes 90 g of methanol was added to the pot. The pot was heated to reflux and 500 g were distilled. A solution of water (124 g) and dichloroacetic acid (0.2 g) were added to the pot and refluxed for 60 minutes. After refluxing, 725 g were distilled and 2-pyrrolidinone (889 g) was added. This synthesis produced a random acrylic polymer of 60 wt % benzyl methacrylate, 20 wt % 2-hydroxyethyl methacrylate, 10 wt % ethyltriethyleneglycol methacrylate and 10 wt % methacrylic acid at a Mn of 5300. The final solution contained 52% polymer solids in 2-pyrrolidinone.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07351278B2uspto-grants-2008_04