bis-(4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluoro-nonyl)-thiocarbamic acid O-(1-methyl-2-phenyl-ethyl) ester

Base Information

Chemical Name:bis-(4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluoro-nonyl)-thiocarbamic acid O-(1-methyl-2-phenyl-ethyl) ester
CAS No.:910660-90-1
Molecular Formula:C₂₈H₂₃F₂₆NOS
Molecular Weight:915.521
Hs Code.:

bis-(4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluoro-nonyl)-thiocarbamic acid <i>O</i>-(1-methyl-2-phenyl-ethyl) ester

Synonyms:bis-(4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluoro-nonyl)-thiocarbamic acid O-(1-methyl-2-phenyl-ethyl) ester

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Chemical Property of bis-(4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluoro-nonyl)-thiocarbamic acid O-(1-methyl-2-phenyl-ethyl) ester

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Technology Process of bis-(4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluoro-nonyl)-thiocarbamic acid O-(1-methyl-2-phenyl-ethyl) ester

There total 8 articles about bis-(4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluoro-nonyl)-thiocarbamic acid O-(1-methyl-2-phenyl-ethyl) ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

: 910660-82-1
C₁₉H₁₂ClF₂₆NS

: 698-87-3,14898-87-4
3-phenyl-2-propanol

: 910660-90-1
bis-(4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluoro-nonyl)-thiocarbamic acid O-(1-methyl-2-phenyl-ethyl) ester

Guidance literature:: With sodium hydride; In tetrahydrofuran; at 20 ℃; for 12h;
DOI:10.1016/j.tetlet.2006.05.142

Reference yield:

: 910660-79-6
benzyl-bis-(4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluoro-nonyl)-amine

: 910660-90-1
bis-(4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluoro-nonyl)-thiocarbamic acid O-(1-methyl-2-phenyl-ethyl) ester

Guidance literature:: Multi-step reaction with 3 steps

1: 87 percent / H₂ / Pd/C / ethyl acetate / 20 °C

2: 47 percent / diethyl ether / -20 °C

3: 100 percent / NaH / tetrahydrofuran / 12 h / 20 °C

With hydrogen; sodium hydride; palladium on activated charcoal; In tetrahydrofuran; diethyl ether; ethyl acetate;
DOI:10.1016/j.tetlet.2006.05.142

Reference yield:

: 38550-44-6
4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluoro-1-iodononan-1-ol

: 910660-90-1
bis-(4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluoro-nonyl)-thiocarbamic acid O-(1-methyl-2-phenyl-ethyl) ester

Guidance literature:: Multi-step reaction with 6 steps

1: 89 percent / LiAlH₄ / tetrahydrofuran

2: 75 percent / PPh₃; I₂; imidazole / CH₂Cl₂ / 0 - 20 °C

3: 76 percent / K₂CO₃ / acetonitrile / 80 °C

4: 87 percent / H₂ / Pd/C / ethyl acetate / 20 °C

5: 47 percent / diethyl ether / -20 °C

6: 100 percent / NaH / tetrahydrofuran / 12 h / 20 °C

With 1H-imidazole; lithium aluminium tetrahydride; hydrogen; iodine; sodium hydride; potassium carbonate; triphenylphosphine; palladium on activated charcoal; In tetrahydrofuran; diethyl ether; dichloromethane; ethyl acetate; acetonitrile;
DOI:10.1016/j.tetlet.2006.05.142