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Benzenepropanoic acid, a-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, (1,1-dimethylethyl)dimethylsilyl ester, (S)-

Base Information Edit
  • Chemical Name:Benzenepropanoic acid, a-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, (1,1-dimethylethyl)dimethylsilyl ester, (S)-
  • CAS No.:89682-03-1
  • Molecular Formula:C21H38O3Si2
  • Molecular Weight:394.702
  • Hs Code.:
  • Mol file:89682-03-1.mol
Benzenepropanoic acid, a-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-,
(1,1-dimethylethyl)dimethylsilyl ester, (S)-

Synonyms:

Suppliers and Price of Benzenepropanoic acid, a-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, (1,1-dimethylethyl)dimethylsilyl ester, (S)-
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Benzenepropanoic acid, a-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, (1,1-dimethylethyl)dimethylsilyl ester, (S)- Edit
Chemical Property:
Purity/Quality:
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MSDS Files:

SDS file from LookChem

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Technology Process of Benzenepropanoic acid, a-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, (1,1-dimethylethyl)dimethylsilyl ester, (S)-

There total 1 articles about Benzenepropanoic acid, a-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, (1,1-dimethylethyl)dimethylsilyl ester, (S)- 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:
With 1H-imidazole; In N,N-dimethyl-formamide; for 21h; Ambient temperature;
DOI:10.1021/jo982376p
Guidance literature:
Multi-step reaction with 6 steps
1: (COCl)2, DMF / CH2Cl2 / 2 h
2: DMAP / CH2Cl2 / 14 h
3: TBAF / tetrahydrofuran / 0.33 h / 0 °C
4: 72 percent / Et3N / CCl4; acetonitrile / 18 h / -10 °C
5: H2 / Pd(OH)2/C / ethanol / 1.5 h
6: acetonitrile
With dmap; oxalyl dichloride; tetrabutyl ammonium fluoride; hydrogen; triethylamine; N,N-dimethyl-formamide; palladium dihydroxide; In tetrahydrofuran; tetrachloromethane; ethanol; dichloromethane; acetonitrile;
DOI:10.1021/jo952074c
Guidance literature:
Multi-step reaction with 7 steps
1: (COCl)2, DMF / CH2Cl2 / 2 h
2: DMAP / CH2Cl2 / 14 h
3: TBAF / tetrahydrofuran / 0.33 h / 0 °C
4: 72 percent / Et3N / CCl4; acetonitrile / 18 h / -10 °C
5: H2 / Pd(OH)2/C / ethanol / 1.5 h
6: acetonitrile
7: 1.) t-BuNH2, 2.) Dowex-Li+ / Heating
With dmap; oxalyl dichloride; Dowex-Li+; tetrabutyl ammonium fluoride; hydrogen; tert-butylamine; triethylamine; N,N-dimethyl-formamide; palladium dihydroxide; In tetrahydrofuran; tetrachloromethane; ethanol; dichloromethane; acetonitrile;
DOI:10.1021/jo952074c
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