methyl 1-[2,4-bis(benzyloxy)cumenyl]-5-[p-(hydroxymethyl)-phenyl]-1H-1,2,3-triazole-4-carboxylate

Base Information

Chemical Name:methyl 1-[2,4-bis(benzyloxy)cumenyl]-5-[p-(hydroxymethyl)-phenyl]-1H-1,2,3-triazole-4-carboxylate
CAS No.:1383717-89-2
Molecular Formula:C₃₄H₃₃N₃O₅
Molecular Weight:563.653
Hs Code.:

Synonyms:methyl 1-[2,4-bis(benzyloxy)cumenyl]-5-[p-(hydroxymethyl)-phenyl]-1H-1,2,3-triazole-4-carboxylate

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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 methyl 1-[2,4-bis(benzyloxy)cumenyl]-5-[p-(hydroxymethyl)-phenyl]-1H-1,2,3-triazole-4-carboxylate

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of methyl 1-[2,4-bis(benzyloxy)cumenyl]-5-[p-(hydroxymethyl)-phenyl]-1H-1,2,3-triazole-4-carboxylate

There total 13 articles about methyl 1-[2,4-bis(benzyloxy)cumenyl]-5-[p-(hydroxymethyl)-phenyl]-1H-1,2,3-triazole-4-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: 80.0%

: 1383717-88-1
methyl 1-[2,4-bis(benzyloxy)cumenyl]-5-[p-(tert-butyldimethylsilyloxymethyl)phenyl]-1H-1,2,3-triazole-4-carboxylate

: 1383717-89-2
methyl 1-[2,4-bis(benzyloxy)cumenyl]-5-[p-(hydroxymethyl)-phenyl]-1H-1,2,3-triazole-4-carboxylate

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 2h;

Reference yield:

: 1383717-87-0
methyl 3-(4-((tert-butyldimethylsilyloxy)methyl)phenyl)-prop-2-ynoate

: 1383717-89-2
methyl 1-[2,4-bis(benzyloxy)cumenyl]-5-[p-(hydroxymethyl)-phenyl]-1H-1,2,3-triazole-4-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: chloro(pentamethylcyclopentadienyl)ruthenium(II) tetramer / N,N-dimethyl-formamide / 20 °C / Inert atmosphere

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C

With tetrabutyl ammonium fluoride; chloro(pentamethylcyclopentadienyl)ruthenium(II) tetramer; In tetrahydrofuran; N,N-dimethyl-formamide;

Reference yield:

: 1093190-17-0
tert-butyl[(4-ethynylphenyl)methoxy]dimethylsilane

: 1383717-89-2
methyl 1-[2,4-bis(benzyloxy)cumenyl]-5-[p-(hydroxymethyl)-phenyl]-1H-1,2,3-triazole-4-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium hexamethyldisilazane / toluene; tetrahydrofuran / 1 h / -78 - -40 °C

1.2: -40 - 20 °C

2.1: chloro(pentamethylcyclopentadienyl)ruthenium(II) tetramer / N,N-dimethyl-formamide / 20 °C / Inert atmosphere

3.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C

With tetrabutyl ammonium fluoride; lithium hexamethyldisilazane; chloro(pentamethylcyclopentadienyl)ruthenium(II) tetramer; In tetrahydrofuran; N,N-dimethyl-formamide; toluene;