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

Propanedioyl dichloride → 5-Ethyl-4-hydroxy-6-methyl-2-pyrone

HRID 323926
노트
인쇄 미리보기

반응식

HRID 323926 반응식
C[Si](C)(C)[O:3][C:4](=[CH:6][CH2:7][CH3:8])[CH3:5].[C:11](Cl)(=[O:16])[CH2:12][C:13](Cl)=[O:14]>CCOCC>[CH2:7]([C:6]1[C:11]([OH:16])=[CH:12][C:13](=[O:14])[O:3][C:4]=1[CH3:5])[CH3:8]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 74269Propanedioyl dichloride2회HCID 545738712-Trimethylsilyloxy-2-pentene

생성물 1

HCID 547031925-Ethyl-4-hydroxy-6-methyl-2-pyrone수율 42.3%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

반응 조건

온도
-78 °C

실험 절차

In 200 mL of ether, was dissolved 13.6 g (85.9 mmol) of 2-trimethylsilyloxy-2-pentene, and 4.6 mL (47.3 mmol) of malonyl chloride was added dropwise to the solution while stirring the solution at −78° C. After the addition of malonyl chloride, the solution was stirred for 1 hour at −78° C., and then, stirred over night while gradually heating the solution to room temperature. The precipitate was filtered and washed with ether. As a result, 3.08 g (20.0 mmol, 42.3%) of 5-ethyl-4-hydroxy-6-methyl-2-pyrone was obtained.

후처리

  1. additionwas added dropwise to the solution
  2. stirringthe solution was stirred for 1 hour at −78° C.
  3. stirringstirred over night
  4. temperaturewhile gradually heating the solution to room temperature
  5. filtrationThe precipitate was filtered
  6. washwashed with ether

출처 및 근거

ORD 기록
ord-68ab7f1ed1cc4277a79de6e3ac3ee3b7
출처 데이터셋
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06215016B1

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트