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5-(2-tert-butyldiphenylsilyloxyethoxymethyl)-3-methoxycarbonylpyridine

Base Information Edit
  • Chemical Name:5-(2-tert-butyldiphenylsilyloxyethoxymethyl)-3-methoxycarbonylpyridine
  • CAS No.:166094-22-0
  • Molecular Formula:C26H31NO4Si
  • Molecular Weight:449.622
  • Hs Code.:
  • Mol file:166094-22-0.mol
5-(2-tert-butyldiphenylsilyloxyethoxymethyl)-3-methoxycarbonylpyridine

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 5-(2-tert-butyldiphenylsilyloxyethoxymethyl)-3-methoxycarbonylpyridine Edit
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Technology Process of 5-(2-tert-butyldiphenylsilyloxyethoxymethyl)-3-methoxycarbonylpyridine

There total 7 articles about 5-(2-tert-butyldiphenylsilyloxyethoxymethyl)-3-methoxycarbonylpyridine 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:
Guidance literature:
Multi-step reaction with 7 steps
1: 97 percent / tetrahydrofuran; diethyl ether / 2 h / Ambient temperature
2: 69 percent / NaBH4 / ethanol / 1.) 0 deg C, 1 h, 2.) room temperature, 3 h, 3.) reflux, 10 h
3: 1.) HCl gas, 2.) SOCl2 / 1.) CH2Cl2, 5 min, 2.) reflux, 2 h
4: 61 percent / HOCH2CH2OH / toluene / 24 h / Ambient temperature
5: 91 percent / imidazole / dimethylformamide / 6 h / Ambient temperature
6: 1.) BuLi / 1.) THF, -78 deg C, 5 min
7: tetrahydrofuran; diethyl ether
With 1H-imidazole; hydrogenchloride; sodium tetrahydroborate; n-butyllithium; thionyl chloride; ethylene glycol; In tetrahydrofuran; diethyl ether; ethanol; N,N-dimethyl-formamide; toluene;
DOI:10.1080/15257779408013225
Guidance literature:
Multi-step reaction with 6 steps
1: 69 percent / NaBH4 / ethanol / 1.) 0 deg C, 1 h, 2.) room temperature, 3 h, 3.) reflux, 10 h
2: 1.) HCl gas, 2.) SOCl2 / 1.) CH2Cl2, 5 min, 2.) reflux, 2 h
3: 61 percent / HOCH2CH2OH / toluene / 24 h / Ambient temperature
4: 91 percent / imidazole / dimethylformamide / 6 h / Ambient temperature
5: 1.) BuLi / 1.) THF, -78 deg C, 5 min
6: tetrahydrofuran; diethyl ether
With 1H-imidazole; hydrogenchloride; sodium tetrahydroborate; n-butyllithium; thionyl chloride; ethylene glycol; In tetrahydrofuran; diethyl ether; ethanol; N,N-dimethyl-formamide; toluene;
DOI:10.1080/15257779408013225
Guidance literature:
Multi-step reaction with 5 steps
1: 1.) HCl gas, 2.) SOCl2 / 1.) CH2Cl2, 5 min, 2.) reflux, 2 h
2: 61 percent / HOCH2CH2OH / toluene / 24 h / Ambient temperature
3: 91 percent / imidazole / dimethylformamide / 6 h / Ambient temperature
4: 1.) BuLi / 1.) THF, -78 deg C, 5 min
5: tetrahydrofuran; diethyl ether
With 1H-imidazole; hydrogenchloride; n-butyllithium; thionyl chloride; ethylene glycol; In tetrahydrofuran; diethyl ether; N,N-dimethyl-formamide; toluene;
DOI:10.1080/15257779408013225
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