(+/-)-methyl 3-((3,5-dichlorophenyl)(methyl)amino)-2-(ethoxycarbonyloxy)cyclopent-1-enecarboxylate

Base Information

Chemical Name:(+/-)-methyl 3-((3,5-dichlorophenyl)(methyl)amino)-2-(ethoxycarbonyloxy)cyclopent-1-enecarboxylate
CAS No.:1364822-58-1
Molecular Formula:C₁₇H₁₉Cl₂NO₅
Molecular Weight:388.248
Hs Code.:

Synonyms:(+/-)-methyl 3-((3,5-dichlorophenyl)(methyl)amino)-2-(ethoxycarbonyloxy)cyclopent-1-enecarboxylate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (+/-)-methyl 3-((3,5-dichlorophenyl)(methyl)amino)-2-(ethoxycarbonyloxy)cyclopent-1-enecarboxylate

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Technology Process of (+/-)-methyl 3-((3,5-dichlorophenyl)(methyl)amino)-2-(ethoxycarbonyloxy)cyclopent-1-enecarboxylate

There total 2 articles about (+/-)-methyl 3-((3,5-dichlorophenyl)(methyl)amino)-2-(ethoxycarbonyloxy)cyclopent-1-enecarboxylate 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: 77.0%

: 1364822-54-7
methyl 3-((3,5-dichlorophenyl)(methyl)amino)-2-oxocyclopentanecarboxylate

: 541-41-3
chloroformic acid ethyl ester

: 1364822-58-1
(+/-)-methyl 3-((3,5-dichlorophenyl)(methyl)amino)-2-(ethoxycarbonyloxy)cyclopent-1-enecarboxylate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In N,N,N,N,N,N-hexamethylphosphoric triamide; at 20 ℃; for 16h; Inert atmosphere;
DOI:10.1021/jo300239e

Reference yield:

: 36596-61-9
methyl 3-bromo-2-oxocyclopentanecarboxylate

: 42266-03-5
3,5-dichloro-N-methylaniline

: 1364822-58-1
(+/-)-methyl 3-((3,5-dichlorophenyl)(methyl)amino)-2-(ethoxycarbonyloxy)cyclopent-1-enecarboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydrogencarbonate / acetonitrile / 16 h / 80 °C / Inert atmosphere

2: N-ethyl-N,N-diisopropylamine / N,N,N,N,N,N-hexamethylphosphoric triamide / 16 h / 20 °C / Inert atmosphere

With sodium hydrogencarbonate; N-ethyl-N,N-diisopropylamine; In N,N,N,N,N,N-hexamethylphosphoric triamide; acetonitrile;
DOI:10.1021/jo300239e