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

2,5-Hexanedione → HCID 12485849, 화합물

HRID 1464350
노트
인쇄 미리보기

반응식

HRID 1464350 반응식
[CH3:1][C:2]1[CH2:6][CH:5]=[CH:4][CH:3]=1.[CH3:7][C:8](=O)[CH2:9][CH2:10][C:11](=O)[CH3:12].[Na]>CO>[CH3:1][C:2]1[C:6]2[C:5](=[C:8]([CH3:7])[CH:9]=[CH:10][C:11]=2[CH3:12])[CH2:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 80352,5-HexanedioneHCID 667751-Methyl-1,3-cyclopentadieneHCID 5360545Sodium

생성물 1

HCID 12485849HCID 12485849, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A mixture of 12 g (150 mmol) of methylcyclopentadiene and 17.1 g (150 mmol) of 2,5-hexanedione was added dropwise to a solution of 8.6 g (975 mmol) of sodium in 200 ml of methanol at 0° C. in the course of 1 hour. After stirring at room temperature for 18 hours, the dark red mixture was poured onto ice-water and extracted with ether. After the extract had been dried over sodium sulfate, the solvent was stripped off and the oil which remained was chromatographed on 600 g of silica gel 60. Using hexane as the mobile phase, first 3.2 g (13%) of 3,4,7-trimethylindene and then 1.5 g (6%) of 2,4,7-trimethylindene were eluted in close succession. Subsequent recrystallization from hexane gave the pure products.

후처리

  1. additionthe dark red mixture was poured onto ice-water
  2. extractionextracted with ether
  3. dry with materialAfter the extract had been dried over sodium sulfate
  4. customthe oil which remained was chromatographed on 600 g of silica gel 60
  5. washUsing hexane as the mobile phase, first 3.2 g (13%) of 3,4,7-trimethylindene and then 1.5 g (6%) of 2,4,7-trimethylindene were eluted in close succession
  6. customSubsequent recrystallization from hexane
  7. customgave the pure products

출처 및 근거

ORD 기록
ord-d139a34cb21d48349720bc39437d467b
출처 데이터셋
uspto-grants-1994_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05304614

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트