<3-(benzyloxy)-2-<3-(benzyloxy)phenyl>-2-methoxy-1-propoxy>-tert-butyldimethylsilane

Base Information

Chemical Name:<3-(benzyloxy)-2-<3-(benzyloxy)phenyl>-2-methoxy-1-propoxy>-tert-butyldimethylsilane
CAS No.:130722-90-6
Molecular Formula:C₃₀H₄₀O₄Si
Molecular Weight:492.731
Hs Code.:

Synonyms:<3-(benzyloxy)-2-<3-(benzyloxy)phenyl>-2-methoxy-1-propoxy>-tert-butyldimethylsilane

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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 <3-(benzyloxy)-2-<3-(benzyloxy)phenyl>-2-methoxy-1-propoxy>-tert-butyldimethylsilane

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Technology Process of <3-(benzyloxy)-2-<3-(benzyloxy)phenyl>-2-methoxy-1-propoxy>-tert-butyldimethylsilane

There total 5 articles about <3-(benzyloxy)-2-<3-(benzyloxy)phenyl>-2-methoxy-1-propoxy>-tert-butyldimethylsilane 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: 70.0%

: 130722-90-6
<3-(benzyloxy)-2-<3-(benzyloxy)phenyl>-2-methoxy-1-propoxy>-tert-butyldimethylsilane

Guidance literature:

Reference yield:

: 13620-31-0
benzyloxyacetonitrile

: 130722-90-6
<3-(benzyloxy)-2-<3-(benzyloxy)phenyl>-2-methoxy-1-propoxy>-tert-butyldimethylsilane

Guidance literature:: Multi-step reaction with 4 steps

1: 2.) 1 N HCl / 1.) THF, 60 deg C, 1 h, 2.) THF, Et₂O, 20 min

2: 2.) NaHCO₃, 30percent H₂O₂ / 1.) THF, RT, 1 h, 2.) MeOH, reflux, overnight

3: 81 percent / imidazole / dimethylformamide / 60 °C

4: 1.) NaH / 1.) DMF, 5 deg C, 1 h, 2.) DMF, from 5 deg C to RT, overnight

With 1H-imidazole; hydrogenchloride; dihydrogen peroxide; sodium hydride; sodium hydrogencarbonate; In N,N-dimethyl-formamide;
DOI:10.1021/jm00092a010

Reference yield:

: 36281-96-6
<3-(benzyloxy)phenyl>magnesium bromide

: 130722-90-6
<3-(benzyloxy)-2-<3-(benzyloxy)phenyl>-2-methoxy-1-propoxy>-tert-butyldimethylsilane

Guidance literature:: Multi-step reaction with 4 steps

1: 2.) 1 N HCl / 1.) THF, 60 deg C, 1 h, 2.) THF, Et₂O, 20 min

2: 2.) NaHCO₃, 30percent H₂O₂ / 1.) THF, RT, 1 h, 2.) MeOH, reflux, overnight

3: 81 percent / imidazole / dimethylformamide / 60 °C

4: 1.) NaH / 1.) DMF, 5 deg C, 1 h, 2.) DMF, from 5 deg C to RT, overnight

With 1H-imidazole; hydrogenchloride; dihydrogen peroxide; sodium hydride; sodium hydrogencarbonate; In N,N-dimethyl-formamide;
DOI:10.1021/jm00092a010