{5-[(4-tert-butyl-phenyl)-(1H-pyrrol-2-yl)-methyl]-1H-pyrrol-2-yl}-(4-trimethylsilanylethynyl-phenyl)-methanol

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Chemical Name:{5-[(4-tert-butyl-phenyl)-(1H-pyrrol-2-yl)-methyl]-1H-pyrrol-2-yl}-(4-trimethylsilanylethynyl-phenyl)-methanol
CAS No.:1026752-63-5
Molecular Formula:C₃₁H₃₆N₂OSi
Molecular Weight:480.725
Hs Code.:

{5-[(4-<i>tert</i>-butyl-phenyl)-(1<i>H</i>-pyrrol-2-yl)-methyl]-1<i>H</i>-pyrrol-2-yl}-(4-trimethylsilanylethynyl-phenyl)-methanol

Synonyms:{5-[(4-tert-butyl-phenyl)-(1H-pyrrol-2-yl)-methyl]-1H-pyrrol-2-yl}-(4-trimethylsilanylethynyl-phenyl)-methanol

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Chemical Property of {5-[(4-tert-butyl-phenyl)-(1H-pyrrol-2-yl)-methyl]-1H-pyrrol-2-yl}-(4-trimethylsilanylethynyl-phenyl)-methanol

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Technology Process of {5-[(4-tert-butyl-phenyl)-(1H-pyrrol-2-yl)-methyl]-1H-pyrrol-2-yl}-(4-trimethylsilanylethynyl-phenyl)-methanol

There total 6 articles about {5-[(4-tert-butyl-phenyl)-(1H-pyrrol-2-yl)-methyl]-1H-pyrrol-2-yl}-(4-trimethylsilanylethynyl-phenyl)-methanol 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:

: 262267-49-2
1-[4-[2-(trimethylsilyl)ethynyl]benzoyl]-5-(4-tert-butylphenyl)dipyrromethane

: 1026752-63-5
{5-[(4-tert-butyl-phenyl)-(1H-pyrrol-2-yl)-methyl]-1H-pyrrol-2-yl}-(4-trimethylsilanylethynyl-phenyl)-methanol

Guidance literature:: With sodium tetrahydroborate; In tetrahydrofuran; methanol;
DOI:10.1021/jo9915473

Reference yield:

: 939-97-9
4-tert-Butylbenzaldehyde

: 1026752-63-5
{5-[(4-tert-butyl-phenyl)-(1H-pyrrol-2-yl)-methyl]-1H-pyrrol-2-yl}-(4-trimethylsilanylethynyl-phenyl)-methanol

Guidance literature:: Multi-step reaction with 3 steps

1: 38 percent / CF₃COOH / 0.08 h

2: 76 percent / EtMgBr / tetrahydrofuran / -78 - 20 °C

3: NaBH₄ / tetrahydrofuran; methanol

With sodium tetrahydroborate; ethylmagnesium bromide; trifluoroacetic acid; In tetrahydrofuran; methanol; 1: Condensation / 2: Acylation / 3: Reduction;
DOI:10.1021/jo9915473

Reference yield:

: 1711-02-0
4-iodobenzoic acid chloride

: 1026752-63-5
{5-[(4-tert-butyl-phenyl)-(1H-pyrrol-2-yl)-methyl]-1H-pyrrol-2-yl}-(4-trimethylsilanylethynyl-phenyl)-methanol

Guidance literature:: Multi-step reaction with 4 steps

1: 91 percent / CH₂Cl₂ / 1.17 h

2: 57 percent / Pd(PPh₃)2Cl₂; CuI; (i-Pr)2NEt / tetrahydrofuran / 24 h / 60 °C

3: 76 percent / EtMgBr / tetrahydrofuran / -78 - 20 °C

4: NaBH₄ / tetrahydrofuran; methanol

With bis-triphenylphosphine-palladium(II) chloride; sodium tetrahydroborate; copper(l) iodide; ethylmagnesium bromide; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; dichloromethane; 1: Acylation / 2: Arylation / 3: Acylation / 4: Reduction;
DOI:10.1021/jo9915473