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

1,6-Dibromohexane → 1-[(2-[(6-Bromohexyl)oxy]ethoxy)methyl]-3-nitrobenzene

HRID 219019
노트
인쇄 미리보기

반응식

HRID 219019 반응식
[N+:1]([C:4]1[CH:5]=[C:6]([CH2:10][O:11][CH2:12][CH2:13][OH:14])[CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2].[Br:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21]Br.[OH-].[Na+]>[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.O>[Br:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][O:14][CH2:13][CH2:12][O:11][CH2:10][C:6]1[CH:7]=[CH:8][CH:9]=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 123681,6-DibromohexaneHCID 14798Sodium HydroxideHCID 121923882-[(3-Nitrophenyl)methoxy]ethanol

생성물 1

HCID 468331061-[(2-[(6-Bromohexyl)oxy]ethoxy)methyl]-3-nitrobenzene수율 68.4%

시약·촉매·용매 2

HCID 74236Tetrabutylammonium Bromide촉매HCID 962
Water
용매

실험 절차

2-{(3-Nitrophenyl)methoxy}ethanol (6.50 g), 1,6-dibromohexane (24.2 g) and tetrabutylammonium bromide (0.21 g) were stirred under nitrogen at 20° and treated with 50% w/v sodium hydroxide (10 ml). The mixture was stirred vigorously for 19 h before water (150 ml) was added. The product was extracted with dichloromethane (3×80 ml) and the combined organic layer was dried (Na2SO4). Solvent evaporation in vacuo gave a residue that was purified by Biotage. Elution with PE-EtOAc (1:0 then 3:1) followed by solvent evaporation in vacuo gave the title compound (8.12 g). HPLC RT=3.238 min.

후처리

  1. additionwas added
  2. extractionThe product was extracted with dichloromethane (3×80 ml)
  3. dry with materialthe combined organic layer was dried (Na2SO4)
  4. customSolvent evaporation in vacuo
  5. customgave a residue that
  6. customwas purified by Biotage
  7. washElution with PE-EtOAc (1:0
  8. custom3:1) followed by solvent evaporation in vacuo

출처 및 근거

ORD 기록
ord-3cb95f37e74d41f48e3c1d99a004708a
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08198483B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트