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

Bromine → Acenaphthene

HRID 569314
노트
인쇄 미리보기

반응식

HRID 569314 반응식
Br[C:2]1[C:12]2=[C:13]3[C:8](=[CH:9][CH:10]=[CH:11]2)[CH:7]=[CH:6][CH:5]=[C:4]3[CH:3]=1.BrBr>>[CH2:3]1[C:4]2=[C:13]3[C:8](=[CH:7][CH:6]=[CH:5]2)[CH:9]=[CH:10][CH:11]=[C:12]3[CH2:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24408BromineHCID 6155531-Bromoacenaphthylene

생성물 1

HCID 6734Acenaphthene

실험 절차

After the reaction solution was cooled, separated potassium bromide was removed by filtration, methanol was distilled, washed 3 times with water, and the benzene solution was concentrated and dropwise added into cold acetone (0°~-10° C.), to obtain reprecipitate of 140 g of condensed bromoacenaphthylene. Elemental analysis showed that the composition of the condensate corresponded to (C12H4.4 Br2.7)m and the yield from acenaphthene was 76.8%.

후처리

  1. temperatureAfter the reaction solution was cooled
  2. customseparated potassium bromide
  3. customwas removed by filtration, methanol
  4. distillationwas distilled
  5. washwashed 3 times with water
  6. concentrationthe benzene solution was concentrated
  7. additiondropwise added into cold acetone (0°~-10° C.)
  8. customto obtain

출처 및 근거

ORD 기록
ord-07350e11e178470888e21a6234197726
출처 데이터셋
uspto-grants-1988_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04731493

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트