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(R)-1-benzyl 7-methyl 5-(tert-butyldimethylsilyloxy)-3-oxoheptanedioate

Base Information Edit
  • Chemical Name:(R)-1-benzyl 7-methyl 5-(tert-butyldimethylsilyloxy)-3-oxoheptanedioate
  • CAS No.:1343494-43-8
  • Molecular Formula:C21H32O6Si
  • Molecular Weight:408.567
  • Hs Code.:
  • Mol file:1343494-43-8.mol
(R)-1-benzyl 7-methyl 5-(tert-butyldimethylsilyloxy)-3-oxoheptanedioate

Synonyms:(R)-1-benzyl 7-methyl 5-(tert-butyldimethylsilyloxy)-3-oxoheptanedioate

Suppliers and Price of (R)-1-benzyl 7-methyl 5-(tert-butyldimethylsilyloxy)-3-oxoheptanedioate
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
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  • price
Total 1 raw suppliers
Chemical Property of (R)-1-benzyl 7-methyl 5-(tert-butyldimethylsilyloxy)-3-oxoheptanedioate Edit
Chemical Property:
Purity/Quality:

98% HPLC *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of (R)-1-benzyl 7-methyl 5-(tert-butyldimethylsilyloxy)-3-oxoheptanedioate

There total 1 articles about (R)-1-benzyl 7-methyl 5-(tert-butyldimethylsilyloxy)-3-oxoheptanedioate 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:
malonic acid monobenzyl ester; With isopropylmagnesium chloride; In tetrahydrofuran; at 0 - 50 ℃; Inert atmosphere;
(R)-3-((tert-butyldimethylsilyl)oxy)-5-(1H-imidazol-1-yl)-5-oxopentanoate methyl ester; In tetrahydrofuran; at 20 ℃; for 12h;
With hydrogenchloride; In tetrahydrofuran; water;
Guidance literature:
Multi-step reaction with 5 steps
1.1: hydrogen / palladium 10% on activated carbon / ethyl acetate / 2 h / 20 °C / Inert atmosphere
2.1: piperidine / N,N-dimethyl-formamide / 10.25 h / 20 - 40 °C / Inert atmosphere
3.1: hydrogenchloride / water; methanol / 0 - 20 °C
4.1: sodium tetrahydroborate; diethyl methoxy borane / tetrahydrofuran; methanol / 0.5 h / -78 °C
4.2: 1 h / 50 °C
5.1: sodium hydroxide; water / methanol / 2 h / 20 °C
With piperidine; hydrogenchloride; sodium tetrahydroborate; diethyl methoxy borane; water; hydrogen; sodium hydroxide; palladium 10% on activated carbon; In tetrahydrofuran; methanol; water; ethyl acetate; N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 7 steps
1.1: hydrogen / palladium 10% on activated carbon / ethyl acetate / 2 h / 20 °C / Inert atmosphere
2.1: piperidine / N,N-dimethyl-formamide / 10.25 h / 20 - 40 °C / Inert atmosphere
3.1: hydrogenchloride / water; methanol / 0 - 20 °C
4.1: sodium tetrahydroborate; diethyl methoxy borane / tetrahydrofuran; methanol / 0.5 h / -78 °C
4.2: 1 h / 50 °C
5.1: sodium hydroxide; water / methanol / 2 h / 20 °C
6.1: hexane; acetone / 16 h / 20 °C
7.1: hydrogenchloride / ethyl acetate; water / pH 4.1
7.2: pH 10
7.3: 16 h / 20 °C
With piperidine; hydrogenchloride; sodium tetrahydroborate; diethyl methoxy borane; water; hydrogen; sodium hydroxide; palladium 10% on activated carbon; In tetrahydrofuran; methanol; hexane; water; ethyl acetate; N,N-dimethyl-formamide; acetone;
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