Acrylic Acid → 1-Butanaminium, N,N,N-tributyl-, 2-propenoate (1:1)

HRID 1078471

反応式

HRID 1078471 の反応式
[C:1]([OH:5])(=[O:4])[CH:2]=[CH2:3].[OH-].[CH2:7]([N+:11]([CH2:20][CH2:21][CH2:22][CH3:23])([CH2:16][CH2:17][CH2:18][CH3:19])[CH2:12][CH2:13][CH2:14][CH3:15])[CH2:8][CH2:9][CH3:10]>>[C:1]([O-:5])(=[O:4])[CH:2]=[CH2:3].[CH2:20]([N+:11]([CH2:7][CH2:8][CH2:9][CH3:10])([CH2:12][CH2:13][CH2:14][CH3:15])[CH2:16][CH2:17][CH2:18][CH3:19])[CH2:21][CH2:22][CH3:23]

参加物

3

反応物 2

HCID 6581Acrylic AcidHCID 2723671Tetrabutylammonium Hydroxide

生成物 1

HCID 30149221-Butanaminium, N,N,N-tributyl-, 2-propenoate (1:1)

反応条件

温度
65 °C

実験手順

A 5 liter glass reaction vessel, fitted with a magnetic stirrer, a hose connector, and a septum were purged with nitrogen. Operating in an atmosphere of nitrogen, 297 grams of poly(isobutylene-co-parabromomethylstyrene) (Mv=1.2M, 1.7% para-bromomethylstyrene) was placed into the vessel along with 3.5 liters of xylenes. The polymer was dissolved with stirring under a partial vacuum of 100 mm Hg with a nitrogen sparge attached at the bottom of the solution. A xylene solution of tetrabutylammonium acrylate was prepared in a second flask under nitrogen by placing 100 ml xylenes, 60 ml tetrabutylammonium hydroxide (1M in methanol) and 6.0 g acrylic acid together with stirring. The contents of the flask was concentrated to half its volume and then diluted to 0.5 liters with more xylenes. This solution was then added to the flask containing the poly(isobutylene-co-para-bromomethylstyrene) and the temperature of the solution was raised to 65° C. The reaction was complete in six hours and the polymer was isolated by precipitation in isopropanol. The polymer was dried in a vacuum oven at 1 mm Hg, 40° C. The analysis for the acrylate content (FTIR and NMR) indicate that the modified polymer has 0.24 meq/gram which is consistent with the complete conversion of acrylic acid to acrylic ester and total conversion of the benzylbromide.

後処理

  1. customfitted with a magnetic stirrer
  2. customa hose connector, and a septum were purged with nitrogen
  3. dissolutionThe polymer was dissolved
  4. customsparge
  5. stirringwith stirring
  6. concentrationThe contents of the flask was concentrated to half its volume
  7. additiondiluted to 0.5 liters with more xylenes
  8. additionThis solution was then added to the flask
  9. additioncontaining the poly(isobutylene-co-para-bromomethylstyrene)
  10. customthe polymer was isolated by precipitation in isopropanol
  11. customThe polymer was dried in a vacuum oven at 1 mm Hg, 40° C

出典と根拠

ORDレコード
ord-ed76edd7d1f64ac68b977bc561e652a7
出典データセット
uspto-grants-1996_08
特許番号
US05548029

関連ノート

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