반응식
C1([Bi](C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1([O:26]C2C=CC=CC=2)C=CC=CC=1.C(O)(=O)CCCCCCC/C=C\CCCCCCCC.C(N)CCCCCCC/C=C\CCCCCCCC.[Se].C(P(CCCCCCCC)CCCCCCCC)CCCCCCC.C([P:106](=[O:123])([CH2:115][CH2:116][CH2:117][CH2:118][CH2:119][CH2:120][CH2:121][CH3:122])[CH2:107][CH2:108][CH2:109][CH2:110][CH2:111][CH2:112][CH2:113][CH3:114])CCCCCCC>C=CCCCCCCCCCCCCCCCC.C1(C)C=CC=CC=1.CO.C(#N)C.CN1CCCC1=O>[CH2:115]([P:106]([CH2:107][CH2:108][CH2:109][CH2:110][CH2:111][CH2:112][CH2:113][CH3:114])(=[O:123])[OH:26])[CH2:116][CH2:117][CH2:118][CH2:119][CH2:120][CH2:121][CH3:122]참가 물질
반응물 7
생성물 1
시약·촉매·용매 5
실험 절차
Materials. 1-methyl-2-pyrrolidinone (99.5%, Aldrich), 1-octadecene (90%, Aldrich), acetonitrile (99.9%, Fisher Chemical), triphenylbismuth (99%, Strem), CdO (99.5%, Aldrich), diphenyl ether (99%, Aldrich), methanol (ACS grade, VWR), oleic acid (90%, Aldrich), oleylamine (70% Aldrich), selenium (99.99%, Strem), trioctylphosphine (90%, Aldrich), trioctylphosphine oxide (99%, Strem), toluene (ACS grade, VWR). 0.2M Se-ODE was prepared by dissolving selenium powder in 1-octadecene at 200° C. for 2 hr under inert atmosphere according to the procedure by Bullen et al.[42]; trioctylphosphine oxide (TOPO) was recrystallized from acetonitrile prior to use; di-n-octylphosphinic acid (DOPA) was synthesized according to the procedure reported by Wang et al.[1]; a stock suspension of 2 mM triphenylbismuth (BiPh3) in 1-octadecene was prepared in advance.
후처리
- custom0.2M Se-ODE was prepared
- customtrioctylphosphine oxide (TOPO) was recrystallized from acetonitrile
- customwas prepared in advance
출처 및 근거
- ORD 기록
- ord-9c3a268df10549b2be3b6aeb3d49fbb1
- 출처 데이터셋
- uspto-grants-2016_04
- 특허 번호
- US09306110B2
연결된 노트
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