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

Hydroquinone → 2-Ethoxy-4-phenyl-3,4-dihydro-2h-pyran

HRID 1413698
노트
인쇄 미리보기

반응식

HRID 1413698 반응식
[CH:1]1[CH:6]=[CH:5][C:4](/[CH:7]=[CH:8]/[CH:9]=[O:10])=[CH:3][CH:2]=1.[CH:11]([O:13][CH2:14][CH3:15])=[CH2:12].C1(C=CC(O)=CC=1)O>>[CH2:11]([O:13][CH:14]1[CH2:15][CH:7]([C:4]2[CH:5]=[CH:6][CH:1]=[CH:2][CH:3]=2)[CH:8]=[CH:9][O:10]1)[CH3:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 785HydroquinoneHCID 8023Ethyl vinyl etherHCID 637511Cinnamaldehyde

생성물 1

HCID 2801772-Ethoxy-4-phenyl-3,4-dihydro-2h-pyran수율 87.2%

실험 절차

313 g (2.37 Mole) of cinnamic aldehyde, 290 g (4.03 Mole) of ethyl vinyl ether and 45 g of hydroquinone were heated at 200° for 16 hours in a 1 l stainless steel autoclave (pressure about 20 atm.). After fractional distillation of the crude material thus obtained, there were isolated 422 g (87% yield) of 2-ethoxy-4-phenyl-3,4-dihydro-2H-pyran, b.p. 89°/0.02 Torr;

후처리

  1. distillationAfter fractional distillation of the crude material
  2. customthus obtained

출처 및 근거

ORD 기록
ord-dbf706e2bceb48ff86549737840f6ea8
출처 데이터셋
uspto-grants-1981_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04251398

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트