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(S)-3,4-dibenzoyloxy-1-(tert-butyldimethylsilyloxy)butan-2-one

Base Information Edit
  • Chemical Name:(S)-3,4-dibenzoyloxy-1-(tert-butyldimethylsilyloxy)butan-2-one
  • CAS No.:247042-38-2
  • Molecular Formula:C24H30O6Si
  • Molecular Weight:442.584
  • Hs Code.:
  • Mol file:247042-38-2.mol
(S)-3,4-dibenzoyloxy-1-(tert-butyldimethylsilyloxy)butan-2-one

Synonyms:(S)-3,4-dibenzoyloxy-1-(tert-butyldimethylsilyloxy)butan-2-one

Suppliers and Price of (S)-3,4-dibenzoyloxy-1-(tert-butyldimethylsilyloxy)butan-2-one
Supply Marketing:Edit
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (S)-3,4-dibenzoyloxy-1-(tert-butyldimethylsilyloxy)butan-2-one Edit
Chemical Property:
Purity/Quality:
Safty Information:
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Technology Process of (S)-3,4-dibenzoyloxy-1-(tert-butyldimethylsilyloxy)butan-2-one

There total 4 articles about (S)-3,4-dibenzoyloxy-1-(tert-butyldimethylsilyloxy)butan-2-one 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 oxalyl dichloride; dimethyl sulfoxide; triethylamine; In dichloromethane; at -60 - 0 ℃; for 1.25h;
DOI:10.1016/S0040-4020(02)01279-6
Guidance literature:
Multi-step reaction with 4 steps
1: 92 percent / Et3N; DMAP / CH2Cl2 / 0 - 20 °C
2: 83 percent / trifluoroacetic acid / 0.5 h / 0 °C
3: 91 percent / imidazole / dimethylformamide / 8 h / 0 °C
4: 80 percent / oxalyl chloride; DMSO; Et3N / CH2Cl2 / 1.25 h / -60 - 0 °C
With 1H-imidazole; dmap; oxalyl dichloride; dimethyl sulfoxide; triethylamine; trifluoroacetic acid; In dichloromethane; N,N-dimethyl-formamide; 4: Swern oxidation;
DOI:10.1016/S0040-4020(02)01279-6
Guidance literature:
Multi-step reaction with 2 steps
1: 91 percent / imidazole / dimethylformamide / 8 h / 0 °C
2: 80 percent / oxalyl chloride; DMSO; Et3N / CH2Cl2 / 1.25 h / -60 - 0 °C
With 1H-imidazole; oxalyl dichloride; dimethyl sulfoxide; triethylamine; In dichloromethane; N,N-dimethyl-formamide; 2: Swern oxidation;
DOI:10.1016/S0040-4020(02)01279-6
upstream raw materials:

C24H32O6Si

benzoyl chloride

C18H18O6

C21H22O6

Downstream raw materials:

C28H40O7Si

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