홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Hydrogen Peroxide → 2-Ethylhexanoic Acid

HRID 1755694
노트
인쇄 미리보기

반응식

HRID 1755694 반응식
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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 5

HCID 784Hydrogen PeroxideHCID 962Water2회HCID 24412Potassium PersulfateHCID 161726(2,2-dibromoethenyl)benzeneHCID 3423265Sodium Lauryl Sulfate

생성물 1

HCID 86972-Ethylhexanoic Acid

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-53d43188c07144a5b3ec5d8467b2908a
출처 데이터셋
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05438096

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트