Technology Process of α-phenyl-β-(4-methoxy-phenyl)-propyl alcohol
There total 5 articles about α-phenyl-β-(4-methoxy-phenyl)-propyl alcohol which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
6b,9a-dimethyl-8-((E)-prop-1-en-1-yl)-6b,9a-dihydroacenaphtho[1,2-d][1,3,2]dioxaborole; phenyllithium;
In
tetrahydrofuran; dibutyl ether;
at 0 - 20 ℃;
for 0.25h;
Inert atmosphere;
Glovebox;
Sealed tube;
4-methoxyphenyl triflate;
With
C64H74FeN2O4P2; palladium diacetate; cesium fluoride;
In
tetrahydrofuran; dibutyl ether;
at 20 ℃;
for 20h;
Inert atmosphere;
Glovebox;
Sealed tube;
With
dihydrogen peroxide; sodium hydroxide;
In
tetrahydrofuran; dibutyl ether; water;
at 0 - 20 ℃;
for 4h;
enantioselective reaction;
Inert atmosphere;
Glovebox;
Sealed tube;
DOI:10.1021/jacs.8b09909
- Guidance literature:
-
With
chlorotriisopropylsilane; 3,5-difluoro-2,4,6-tris(N-phenylanilino)benzonitrile; potassium carbonate;
In
acetonitrile;
at 25 ℃;
for 16h;
Photolysis;
Molecular sieve;
DOI:10.1039/c9sc04987h
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: 1H-imidazole; iron(III) chloride / acetonitrile / 1 h / 20 °C / Inert atmosphere
2.1: tetrahydrofuran; dibutyl ether / 0.25 h / 0 - 20 °C / Inert atmosphere; Glovebox; Sealed tube
2.2: 20 h / 20 °C / Inert atmosphere; Glovebox; Sealed tube
2.3: 4 h / 0 - 20 °C / Inert atmosphere; Glovebox; Sealed tube
With
1H-imidazole; iron(III) chloride;
In
tetrahydrofuran; dibutyl ether; acetonitrile;
DOI:10.1021/jacs.8b09909