methyl 4-(4-fluorophenyl)-2-methylbut-3-yn-2-yl(3-hydroxy-5-methyl-3-phenylhex-5-enyl)carbamate

Base Information

Chemical Name:methyl 4-(4-fluorophenyl)-2-methylbut-3-yn-2-yl(3-hydroxy-5-methyl-3-phenylhex-5-enyl)carbamate
CAS No.:1262298-49-6
Molecular Formula:C₂₆H₃₀FNO₃
Molecular Weight:423.528
Hs Code.:

Synonyms:methyl 4-(4-fluorophenyl)-2-methylbut-3-yn-2-yl(3-hydroxy-5-methyl-3-phenylhex-5-enyl)carbamate

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Chemical Property of methyl 4-(4-fluorophenyl)-2-methylbut-3-yn-2-yl(3-hydroxy-5-methyl-3-phenylhex-5-enyl)carbamate

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Technology Process of methyl 4-(4-fluorophenyl)-2-methylbut-3-yn-2-yl(3-hydroxy-5-methyl-3-phenylhex-5-enyl)carbamate

There total 4 articles about methyl 4-(4-fluorophenyl)-2-methylbut-3-yn-2-yl(3-hydroxy-5-methyl-3-phenylhex-5-enyl)carbamate 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: 73.0%

: 1262298-47-4
methyl 3-hydroxy-5-methyl-3-phenylhex-5-enyl(2-methylbut-3-yn-2-yl)carbamate

: 460-00-4
1-Bromo-4-fluorobenzene

: 1262298-49-6
methyl 4-(4-fluorophenyl)-2-methylbut-3-yn-2-yl(3-hydroxy-5-methyl-3-phenylhex-5-enyl)carbamate

Guidance literature:: With copper(l) iodide; triethylamine; bis-triphenylphosphine-palladium(II) chloride; at 100 ℃; for 2h; Inert atmosphere; microwave;

Reference yield:

: 936-59-4
3-chloropropiophenone

: 1262298-49-6
methyl 4-(4-fluorophenyl)-2-methylbut-3-yn-2-yl(3-hydroxy-5-methyl-3-phenylhex-5-enyl)carbamate

Guidance literature:: Multi-step reaction with 4 steps

1.1: diisobutylaluminium hydride; magnesium / hexane; tetrahydrofuran / 2 h / 20 - 30 °C / Inert atmosphere

1.2: 0.5 h / 0 °C / Inert atmosphere

1.3: 30 °C

2.1: potassium iodide; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 24 h / 80 °C

3.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / Cooling

3.2: 20 °C

4.1: triethylamine; copper(l) iodide / bis-triphenylphosphine-palladium(II) chloride / 2 h / 100 °C / Inert atmosphere; microwave

With copper(l) iodide; diisobutylaluminium hydride; magnesium; triethylamine; N-ethyl-N,N-diisopropylamine; potassium iodide; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; hexane; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1110641-65-0
1-chloro-5-methyl-3-phenylhex-5-en-3-ol

: 1262298-49-6
methyl 4-(4-fluorophenyl)-2-methylbut-3-yn-2-yl(3-hydroxy-5-methyl-3-phenylhex-5-enyl)carbamate

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium iodide; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 24 h / 80 °C

2.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / Cooling

2.2: 20 °C

3.1: triethylamine; copper(l) iodide / bis-triphenylphosphine-palladium(II) chloride / 2 h / 100 °C / Inert atmosphere; microwave

With copper(l) iodide; triethylamine; N-ethyl-N,N-diisopropylamine; potassium iodide; bis-triphenylphosphine-palladium(II) chloride; In dichloromethane; N,N-dimethyl-formamide;