(R)-tert-butyl 2-(2-ethoxy-1-hydroxy-2-oxoethyl)-5-phenyl-1H-pyrrole-1-carboxylate

Base Information

Chemical Name:(R)-tert-butyl 2-(2-ethoxy-1-hydroxy-2-oxoethyl)-5-phenyl-1H-pyrrole-1-carboxylate
CAS No.:1623145-91-4
Molecular Formula:C₁₉H₂₃NO₅
Molecular Weight:345.395
Hs Code.:

Synonyms:(R)-tert-butyl 2-(2-ethoxy-1-hydroxy-2-oxoethyl)-5-phenyl-1H-pyrrole-1-carboxylate

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Chemical Property of (R)-tert-butyl 2-(2-ethoxy-1-hydroxy-2-oxoethyl)-5-phenyl-1H-pyrrole-1-carboxylate

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Technology Process of (R)-tert-butyl 2-(2-ethoxy-1-hydroxy-2-oxoethyl)-5-phenyl-1H-pyrrole-1-carboxylate

There total 3 articles about (R)-tert-butyl 2-(2-ethoxy-1-hydroxy-2-oxoethyl)-5-phenyl-1H-pyrrole-1-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:

: 1623146-26-8
C₂₂H₃₁NO₅Si

: 1623145-91-4
(R)-tert-butyl 2-(2-ethoxy-1-hydroxy-2-oxoethyl)-5-phenyl-1H-pyrrole-1-carboxylate

Guidance literature:: With hydrogenchloride; In tetrahydrofuran; water; at 20 ℃; for 1h;
DOI:10.1016/j.tetasy.2014.06.013

Reference yield:

: 1623145-34-5
tert-butyl 2-phenyl-5-(trimethylsilyl)-1H-pyrrole-1-carboxylate

: 1623145-91-4
(R)-tert-butyl 2-(2-ethoxy-1-hydroxy-2-oxoethyl)-5-phenyl-1H-pyrrole-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: C₄₄H₃₂P₂Pd⁽²⁺⁾*2F₆Sb^(1-) / dichloromethane / 24 h / -40 °C

2: hydrogenchloride / tetrahydrofuran; water / 1 h / 20 °C

With hydrogenchloride; C₄₄H₃₂P₂Pd⁽²⁺⁾*2F₆Sb^(1-); In tetrahydrofuran; dichloromethane; water; 1: |Friedel-Crafts Alkylation;
DOI:10.1016/j.tetasy.2014.06.013

Reference yield:

: 163525-97-1
tert-butyl 2-phenyl-1H-pyrrole-1-carboxylate

: 1623145-91-4
(R)-tert-butyl 2-(2-ethoxy-1-hydroxy-2-oxoethyl)-5-phenyl-1H-pyrrole-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: n-butyllithium; diisopropylamine / tetrahydrofuran; hexane / 6.33 h / -78 °C

1.2: -78 - 0 °C

2.1: C₄₄H₃₂P₂Pd⁽²⁺⁾*2F₆Sb^(1-) / dichloromethane / 24 h / -40 °C

3.1: hydrogenchloride / tetrahydrofuran; water / 1 h / 20 °C

With hydrogenchloride; n-butyllithium; C₄₄H₃₂P₂Pd⁽²⁺⁾*2F₆Sb^(1-); diisopropylamine; In tetrahydrofuran; hexane; dichloromethane; water; 2.1: |Friedel-Crafts Alkylation;
DOI:10.1016/j.tetasy.2014.06.013