3-(4-chloro-phenyl)-2,3-dihydro-pyrrole-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:3-(4-chloro-phenyl)-2,3-dihydro-pyrrole-1-carboxylic acid tert-butyl ester
CAS No.:911464-87-4
Molecular Formula:C₁₅H₁₈ClNO₂
Molecular Weight:279.766
Hs Code.:

3-(4-chloro-phenyl)-2,3-dihydro-pyrrole-1-carboxylic acid <i>tert</i>-butyl ester

Synonyms:3-(4-chloro-phenyl)-2,3-dihydro-pyrrole-1-carboxylic acid tert-butyl ester

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Chemical Property of 3-(4-chloro-phenyl)-2,3-dihydro-pyrrole-1-carboxylic acid tert-butyl ester

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Technology Process of 3-(4-chloro-phenyl)-2,3-dihydro-pyrrole-1-carboxylic acid tert-butyl ester

There total 6 articles about 3-(4-chloro-phenyl)-2,3-dihydro-pyrrole-1-carboxylic acid tert-butyl 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: 64.0%

: [(E)-(R)-2,4-Bis-(4-chloro-phenyl)-but-3-enyl]-vinyl-carbamic acid tert-butyl ester

: 911464-87-4
3-(4-chloro-phenyl)-2,3-dihydro-pyrrole-1-carboxylic acid tert-butyl ester

: 3-(4-chloro-phenyl)-2,5-dihydro-pyrrole-1-carboxylic acid tert-butyl ester

Guidance literature:: Grubbs catalyst first generation; In tetrahydrofuran; for 24h; Heating;
DOI:10.1016/j.tetlet.2006.07.029

Reference yield:

: 911465-10-6
C₁₆H₁₃Cl₂NO₂

: 911464-87-4
3-(4-chloro-phenyl)-2,3-dihydro-pyrrole-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: SmI₂ / methanol; tetrahydrofuran / 4 h / 0 °C

1.2: 95 percent / NEt₃ / methanol / 1 h / 20 °C

2.1: 71 percent / (bathophenanthroline)palladium(II) trifluoroacetate complex / 1,2-dimethoxy-ethane / 24 h / 80 °C

3.1: 21 percent / Grubbs catalyst / 1,2-dichloro-ethane / 24 h / Heating

With samarium diiodide; Grubbs catalyst first generation; (bathophenanthroline)palladium(II) trifluoroacetate; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; 1,2-dichloro-ethane;
DOI:10.1016/j.tetlet.2006.07.029

Reference yield:

: 911464-93-2
Carbonic acid (E)-1,3-bis-(4-chloro-phenyl)-allyl ester ethyl ester

: 911464-87-4
3-(4-chloro-phenyl)-2,3-dihydro-pyrrole-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: 92 percent / aspartic acid-derived P-chirogenic diaminophosphine oxide; BSA; iPr2NEt / (η³-C3H5PdCl)2 / 3 h / 20 °C

2.1: SmI₂ / methanol; tetrahydrofuran / 4 h / 0 °C

2.2: 95 percent / NEt₃ / methanol / 1 h / 20 °C

3.1: 71 percent / (bathophenanthroline)palladium(II) trifluoroacetate complex / 1,2-dimethoxy-ethane / 24 h / 80 °C

4.1: 21 percent / Grubbs catalyst / 1,2-dichloro-ethane / 24 h / Heating

With benzenesulfonamide; samarium diiodide; aspartic acid-derived P-chirogenic diaminophosphine oxide; N-ethyl-N,N-diisopropylamine; Grubbs catalyst first generation; bis(η3-allyl-μ-chloropalladium(II)); (bathophenanthroline)palladium(II) trifluoroacetate; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; 1,2-dichloro-ethane;
DOI:10.1016/j.tetlet.2006.07.029