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

Epichlorohydrin → HCID 21490522, 화합물

HRID 1973769
노트
인쇄 미리보기

반응식

HRID 1973769 반응식
[CH:1]([C:4]1[CH:10]=[CH:9][CH:8]=[C:6]([OH:7])[C:5]=1[OH:11])([CH3:3])[CH3:2].[CH2:12]([CH:14]1[O:16][CH2:15]1)[Cl:13].[OH-:17].[Na+]>O>[CH:1]([C:4]1[C:5]([O:11][CH2:15][CH:14]([OH:16])[CH2:12][Cl:13])=[C:6]([O:7][CH2:15][CH:14]([OH:17])[CH2:12][Cl:13])[CH:8]=[CH:9][CH:10]=1)([CH3:3])[CH3:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7835EpichlorohydrinHCID 14798Sodium HydroxideHCID 164983-Isopropylcatechol

생성물 1

HCID 21490522HCID 21490522, 화합물

시약·촉매·용매 1

HCID 962Water촉매

반응 조건

온도
40 °C

실험 절차

22.9 g. of 3-isopropylcatechol, 56 g. of epichlorhydrin and 0.2 g. of sodium hydroxide, dissolved in a few drops of water, are stirred together for 21 days at 40° C under a nitrogen atmosphere. The excess of epichlorohydrin is distilled off under reduced pressure. The resulting oil is dissolved in chloroform, washed twice with water and purified by molecular distillation at 10-3 mm.Hg 32.55 g. of impure 1,1'-[(3-isopropyl-o-phenylene)dioxy]-bis-(3-chloropropan-2-ol) are obtained.

후처리

  1. distillationThe excess of epichlorohydrin is distilled off under reduced pressure
  2. dissolutionThe resulting oil is dissolved in chloroform
  3. washwashed twice with water
  4. distillationpurified by molecular distillation at 10-3 mm.Hg 32.55 g

출처 및 근거

ORD 기록
ord-b0447b2b57c04281a759f36bbb7b6117
출처 데이터셋
uspto-grants-1976_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03998874

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트