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Hydrogen Peroxide → 2-Ethylhexanoic Acid

HRID 1755694
ノート
印刷プレビュー

反応式

HRID 1755694 の反応式
Br[C:2](Br)=[CH:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.S([O-])(OCCCCCCCCCCCC)(=O)=[O:12].[Na+].S(OOS([O-])(=O)=O)([O-])(=O)=O.[K+].[K+].OO.[OH2:43]>>[CH3:8][CH2:7][CH2:6][CH2:5][CH:4]([C:9]([OH:12])=[O:43])[CH2:3][CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 5

HCID 784Hydrogen PeroxideHCID 962Water2 回HCID 24412Potassium PersulfateHCID 161726(2,2-dibromoethenyl)benzeneHCID 3423265Sodium Lauryl Sulfate

生成物 1

HCID 86972-Ethylhexanoic Acid

実験手順

A series of emulsion polymerizations of dibromostyrene (DBS)/2-ethylhexyl acrylate (2-EHA) were carried out in 8 oz. bottles. All the ingredients (122.50 or 180 parts by weight deionized water, 3 parts sodium dodecyl sulfate, 0.3 parts potassium persulfate, 0.2 parts t-dodecyl mercaptan and 100 parts total monomers in the ratio desired in the polymer) were charged into 8 oz. bottles and flushes well with nitrogen, and then reacted at 50° C. to about 45.8 or 36.5% solids in 15 hr. The whole bottle was cooled to room temperature and 3 parts deionized water and 0.18 parts 50% H2O2 added, followed by agitation for 20 minutes. The results of these preparations are set forth in Table I. The latices in Examples 1 and 2 perform well in a variety of coating applications, and display improved flame retardancy, while the latices in Examples 3 through 5 give very soft and tacky coatings.

後処理

  1. additionwere charged into 8 oz. bottles and flushes well with nitrogen
  2. additionadded
  3. customThe results of these preparations
  4. temperatureimproved flame retardancy
  5. customwhile the latices in Examples 3 through 5 give very soft

出典と根拠

ORDレコード
ord-53d43188c07144a5b3ec5d8467b2908a
出典データセット
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05438096

反応ノート

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