{3-[(3,5-bis-{3-[(3,5-dimethoxy-phenyl)-p-tolyl-amino]-benzyloxy}-phenyl)-p-tolyl-amino]-phenyl}-methanol

Base Information

Chemical Name:{3-[(3,5-bis-{3-[(3,5-dimethoxy-phenyl)-p-tolyl-amino]-benzyloxy}-phenyl)-p-tolyl-amino]-phenyl}-methanol
CAS No.:351340-91-5
Molecular Formula:C₆₄H₆₁N₃O₇
Molecular Weight:984.204
Hs Code.:

{3-[(3,5-bis-{3-[(3,5-dimethoxy-phenyl)-<i>p</i>-tolyl-amino]-benzyloxy}-phenyl)-<i>p</i>-tolyl-amino]-phenyl}-methanol

Synonyms:{3-[(3,5-bis-{3-[(3,5-dimethoxy-phenyl)-p-tolyl-amino]-benzyloxy}-phenyl)-p-tolyl-amino]-phenyl}-methanol

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Chemical Property of {3-[(3,5-bis-{3-[(3,5-dimethoxy-phenyl)-p-tolyl-amino]-benzyloxy}-phenyl)-p-tolyl-amino]-phenyl}-methanol

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Technology Process of {3-[(3,5-bis-{3-[(3,5-dimethoxy-phenyl)-p-tolyl-amino]-benzyloxy}-phenyl)-p-tolyl-amino]-phenyl}-methanol

There total 12 articles about {3-[(3,5-bis-{3-[(3,5-dimethoxy-phenyl)-p-tolyl-amino]-benzyloxy}-phenyl)-p-tolyl-amino]-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: 63.0%

: 351340-90-4
3,5-dimethoxy-4'-methyl-3''-bromomethyltriphenylamine

: 351340-87-9
3,5-dihydroxy-4'-methyl-3''-hydroxymethyltriphenylamine

: 351340-91-5
{3-[(3,5-bis-{3-[(3,5-dimethoxy-phenyl)-p-tolyl-amino]-benzyloxy}-phenyl)-p-tolyl-amino]-phenyl}-methanol

Guidance literature:: With 18-crown-6 ether; potassium carbonate; In tetrahydrofuran; for 20h; Heating;
DOI:10.1021/ol0160203

Reference yield:

: 106-38-7
para-bromotoluene

: 351340-91-5
{3-[(3,5-bis-{3-[(3,5-dimethoxy-phenyl)-p-tolyl-amino]-benzyloxy}-phenyl)-p-tolyl-amino]-phenyl}-methanol

Guidance literature:: Multi-step reaction with 6 steps

1.1: NaO-t-Bu / tris(dibenzylideneacetone)palladium; bis(diphenylphosphino)ferrocene / toluene / 5 h / 90 °C

2.1: 4.96 g / NaO-t-Bu / tris(dibenzylideneacetone)palladium; bis(diphenylphosphino)ferrocene / toluene / 48 h / 90 °C

3.1: t-BuLi / tetrahydrofuran / 0.25 h

3.2: 81 percent / tetrahydrofuran / 20 h / 20 °C

4.1: 95 percent / NaBH₄ / ethanol / 8 h

5.1: 69 percent / CBr₄; PPh₃ / tetrahydrofuran

6.1: 63 percent / K₂CO₃; 18-crown-6 / tetrahydrofuran / 20 h / Heating

With sodium tetrahydroborate; 18-crown-6 ether; carbon tetrabromide; tert.-butyl lithium; potassium carbonate; triphenylphosphine; sodium t-butanolate; 1,1'-bis(diphenylphosphino)ferrocene; tris(dibenzylideneacetone)palladium; In tetrahydrofuran; ethanol; toluene;
DOI:10.1021/ol0160203

Reference yield:

: 108-36-1
1,3-dibromobenzene

: 351340-91-5
{3-[(3,5-bis-{3-[(3,5-dimethoxy-phenyl)-p-tolyl-amino]-benzyloxy}-phenyl)-p-tolyl-amino]-phenyl}-methanol

Guidance literature:: Multi-step reaction with 5 steps

1.1: 4.96 g / NaO-t-Bu / tris(dibenzylideneacetone)palladium; bis(diphenylphosphino)ferrocene / toluene / 48 h / 90 °C

2.1: t-BuLi / tetrahydrofuran / 0.25 h

2.2: 81 percent / tetrahydrofuran / 20 h / 20 °C

3.1: 95 percent / NaBH₄ / ethanol / 8 h

4.1: 69 percent / CBr₄; PPh₃ / tetrahydrofuran

5.1: 63 percent / K₂CO₃; 18-crown-6 / tetrahydrofuran / 20 h / Heating

With sodium tetrahydroborate; 18-crown-6 ether; carbon tetrabromide; tert.-butyl lithium; potassium carbonate; triphenylphosphine; sodium t-butanolate; 1,1'-bis(diphenylphosphino)ferrocene; tris(dibenzylideneacetone)palladium; In tetrahydrofuran; ethanol; toluene;
DOI:10.1021/ol0160203