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

Epichlorohydrin → HCID 20496759, 화합물

HRID 1074457
노트
인쇄 미리보기

반응식

HRID 1074457 반응식
[OH:1][C:2]1[CH:17]=[CH:16][C:5]2[CH2:6][CH:7]([C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=3)[CH2:8][O:9][C:4]=2[CH:3]=1.N1CCCCC1.Cl[CH2:25][CH:26]1[O:28][CH2:27]1>>[O:28]1[CH:26]([CH2:25][O:1][C:2]2[CH:17]=[CH:16][C:5]3[CH2:6][CH:7]([C:10]4[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=4)[CH2:8][O:9][C:4]=3[CH:3]=2)[CH2:27]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 7835EpichlorohydrinHCID 8082PiperidineHCID 204967613-Phenylchroman-7-ol

생성물 1

HCID 20496759HCID 20496759, 화합물

실험 절차

17 g 7-hydroxy-3-phenyl-3,4-dihydro-2H-1-benzopyrane, 0.1 cm3 piperidine and 100 cm3 1-chloro-2,3-epoxypropane were stirred for 6 hours at a temperature of 90° C. The solution was evaporated under reduced pressure, the residue was dissolved in 150 cm3 benzene and the obtained solution was extracted twice with 25--25 cm3 saturated sodium carbonate solution. The benzene phase was separated from the precipitated resin, clarificated with charcoal, filtered and evaporated. Crystallizing the residue from methanol, 15 g pure crystalline 1,2-epoxy-3-(3-phenyl-3,4-dihydro-2H-1-benzopyrane-7-yloxy)-propane was obtained (m.p. 117°-119° C.).

후처리

  1. custom
The solution was evaporated under reduced pressure
  • dissolutionthe residue was dissolved in 150 cm3 benzene
  • extractionthe obtained solution was extracted twice with 25--25 cm3 saturated sodium carbonate solution
  • customThe benzene phase was separated from the precipitated resin
  • filtrationfiltered
  • customevaporated
  • customCrystallizing the residue from methanol
  • 출처 및 근거

    ORD 기록
    ord-e2d1ffefd2ad4a80a2193f334e7eb777
    출처 데이터셋
    uspto-grants-1983_07
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04391821

    반응 노트

    불러오는 중…

    이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트