(R)-5-(3,4,5-trifluorophenyl)-3,4-dihydro-2H-pyrrole-2-carboxylic acid ethyl ester

Base Information

Chemical Name:(R)-5-(3,4,5-trifluorophenyl)-3,4-dihydro-2H-pyrrole-2-carboxylic acid ethyl ester
CAS No.:1050393-51-5
Molecular Formula:C₁₃H₁₂F₃NO₂
Molecular Weight:271.239
Hs Code.:

Synonyms:(R)-5-(3,4,5-trifluorophenyl)-3,4-dihydro-2H-pyrrole-2-carboxylic acid ethyl ester

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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 (R)-5-(3,4,5-trifluorophenyl)-3,4-dihydro-2H-pyrrole-2-carboxylic acid ethyl ester

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Technology Process of (R)-5-(3,4,5-trifluorophenyl)-3,4-dihydro-2H-pyrrole-2-carboxylic acid ethyl ester

There total 5 articles about (R)-5-(3,4,5-trifluorophenyl)-3,4-dihydro-2H-pyrrole-2-carboxylic acid 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:

: 68766-96-1
ethyl (R)-2-pyrrolidone-5-carboxylate

: 1050393-51-5
(R)-5-(3,4,5-trifluorophenyl)-3,4-dihydro-2H-pyrrole-2-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine / dmap / tetrahydrofuran / 5 h / 20 °C

1.2: 0.5 h / 20 °C

2.1: tetrahydrofuran / 1 h / -40 °C

3.1: hydrogenchloride / ethyl acetate / 3 h / 20 °C

With hydrogenchloride; triethylamine; dmap; In tetrahydrofuran; ethyl acetate;

Reference yield:

: 937400-23-2
(R)-2-tert-butoxycarbonylamino-5-oxo-5-(3,4,5-trifluorophenyl)pentanoic acid ethyl ester

: 1050393-51-5
(R)-5-(3,4,5-trifluorophenyl)-3,4-dihydro-2H-pyrrole-2-carboxylic acid ethyl ester

Guidance literature:: With hydrogenchloride; In ethyl acetate; at 20 ℃; for 3h;

Reference yield:

: 138526-69-9
3,4,5-trifluoro-1-bromobenzene

: 1050393-51-5
(R)-5-(3,4,5-trifluorophenyl)-3,4-dihydro-2H-pyrrole-2-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: magnesium / iodine / diethyl ether / 1 - 1.5 h / 20 °C / Heating / reflux

2: tetrahydrofuran / 1 h / -40 °C

3: hydrogenchloride / ethyl acetate / 3 h / 20 °C

With hydrogenchloride; magnesium; iodine; In tetrahydrofuran; diethyl ether; ethyl acetate;