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

Styrene → Benzene, ethenyl-, polymer with 1,3-butadiene

HRID 353650
노트
인쇄 미리보기

반응식

HRID 353650 반응식
[CH2:1]=[CH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[CH2:9]=[CH:10][CH:11]=[CH2:12].CN(CCN(C)C)C.[Li]CCCC>>[CH2:1]=[CH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[CH2:9]=[CH:10][CH:11]=[CH2:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 7501StyreneHCID 78451,3-ButadieneHCID 8037N,N,N',N'-TetramethylethylenediamineHCID 178418339Butyllithium

생성물 1

HCID 62697Benzene, ethenyl-, polymer with 1,3-butadiene

실험 절차

In this example, a 1/11/88 PES/styrene/1,3-butadiene terpolymer was prepared using the procedure described in Example 34 except that the ratio of PES to styrene and to 1,3-butadiene was changed to 1:11:80 and the molar ratio of TMEDA to n-BuLi was also changed to 1:1. GC analysis of residual monomer with respect to polymerization time indicated that PES was randomly distributed along the polymer chain. The resulting terpolymer had a Tg at −42° C. and was determined to a have a ML-4 of 47.

후처리

  1. customGC analysis of residual monomer with respect to polymerization time
  2. customat −42° C.

출처 및 근거

ORD 기록
ord-53e0851c347d4509bc52251a0e84c4f5
출처 데이터셋
uspto-grants-2004_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06753447B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트