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

Hexachlorocyclopentadiene → HCID 13153833, 화합물

HRID 1646714
노트
인쇄 미리보기

반응식

HRID 1646714 반응식
[Cl:1]C1(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl.ClCl.[Cl:14][C:15]1[C:19]([F:21])([F:20])[C:18]([Cl:23])(F)[C:17]([F:25])([F:24])[C:16]=1[Cl:26]>>[Cl:14][C:15]1[C:19]([F:21])([F:20])[C:18]([Cl:1])([Cl:23])[C:17]([F:25])([F:24])[C:16]=1[Cl:26]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6478HexachlorocyclopentadieneHCID 24526ChlorineHCID 11086552HCID 11086552, 화합물

생성물 1

HCID 13153833HCID 13153833, 화합물수율 9.7%

실험 절차

200 g of HF were passed over 140 ml of this catalyst at 360° C. in the course of 6 hours. 102 g of hexachlorocyclopentadiene, 170 g of HF and 23 g of chlorine were then passed over at 350° C. in the course of 5 hours. The reaction gases were condensed in ice-water. 85.4 g of an organic phase which contained 60.5% of 1,2-dichloro-3,3,4,4,5,5-pentafluorocyclopent-1-ene, 23.5% of 1,2,4-trichloro-3,3,4,5,5-pentafluorocyclopent-1-ene (and isomers as in Example 1) and 9.7% of 1,2,4,4-tetrachloro-3,3,5,5-tetrafluorocyclopent-1-ene (and isomers as in Example 1) were formed. The hexachlorocyclopentadiene content in the reaction product was 0.1%.

후처리

  1. customwere then passed over at 350° C. in the course of 5 hours
  2. customThe reaction gases

출처 및 근거

ORD 기록
ord-099d933a094e4693870666c60cbeb297
출처 데이터셋
uspto-grants-1993_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05180861

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트