(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 2-phenyl-4-(3,4,5-trichloro-phenyl)-4-(trifluoromethyl)-3,4-dihydro-2H-pyrrole-3-carboxylate

Base Information

Chemical Name:(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 2-phenyl-4-(3,4,5-trichloro-phenyl)-4-(trifluoromethyl)-3,4-dihydro-2H-pyrrole-3-carboxylate
CAS No.:1350476-11-7
Molecular Formula:C₂₈H₂₉Cl₃F₃NO₂
Molecular Weight:574.898
Hs Code.:

Synonyms:(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 2-phenyl-4-(3,4,5-trichloro-phenyl)-4-(trifluoromethyl)-3,4-dihydro-2H-pyrrole-3-carboxylate

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Chemical Property of (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 2-phenyl-4-(3,4,5-trichloro-phenyl)-4-(trifluoromethyl)-3,4-dihydro-2H-pyrrole-3-carboxylate

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Technology Process of (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 2-phenyl-4-(3,4,5-trichloro-phenyl)-4-(trifluoromethyl)-3,4-dihydro-2H-pyrrole-3-carboxylate

There total 4 articles about (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 2-phenyl-4-(3,4,5-trichloro-phenyl)-4-(trifluoromethyl)-3,4-dihydro-2H-pyrrole-3-carboxylate 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: 33.0%

: 88333-03-3,10340-91-7
Benzyl isocyanide

: 1350374-96-7
(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl (2E)-4,4,4-trifluoro-3-(3,4,5-trichloro-phenyl)but-2-enoate

: 1350476-11-7
(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 2-phenyl-4-(3,4,5-trichloro-phenyl)-4-(trifluoromethyl)-3,4-dihydro-2H-pyrrole-3-carboxylate

Guidance literature:: copper(II) oxide; In toluene; for 6h; Reflux;

Reference yield:

: C₁₀H₃Cl₄F₃O

: 1350476-11-7
(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 2-phenyl-4-(3,4,5-trichloro-phenyl)-4-(trifluoromethyl)-3,4-dihydro-2H-pyrrole-3-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 20 °C / Cooling with ice

2: copper(II) oxide / toluene / 6 h / Reflux

With triethylamine; copper(II) oxide; In dichloromethane; toluene;

Reference yield:

: 158401-00-4
1-(3,4,5-trichloro-phenyl)-2,2,2-trifluoro-ethanone

: 1350476-11-7
(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 2-phenyl-4-(3,4,5-trichloro-phenyl)-4-(trifluoromethyl)-3,4-dihydro-2H-pyrrole-3-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium acetate / 5 h / 100 °C

1.2: 4 - 20 °C

2.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 1 h / 20 °C

3.1: triethylamine / dichloromethane / 20 °C / Cooling with ice

4.1: copper(II) oxide / toluene / 6 h / Reflux

With oxalyl dichloride; sodium acetate; triethylamine; N,N-dimethyl-formamide; copper(II) oxide; In dichloromethane; toluene;