methyl (3S,5R)-5-[(tert-butyldimethylsilyl)oxy]-3-[(p-nitrophenylcarbonyl)oxy]cyclohex-1-enecarboxylate

Base Information

Chemical Name:methyl (3S,5R)-5-[(tert-butyldimethylsilyl)oxy]-3-[(p-nitrophenylcarbonyl)oxy]cyclohex-1-enecarboxylate
CAS No.:301153-82-2
Molecular Formula:C₂₁H₂₉NO₇Si
Molecular Weight:435.549
Hs Code.:

Synonyms:methyl (3S,5R)-5-[(tert-butyldimethylsilyl)oxy]-3-[(p-nitrophenylcarbonyl)oxy]cyclohex-1-enecarboxylate

Suppliers and Price of methyl (3S,5R)-5-[(tert-butyldimethylsilyl)oxy]-3-[(p-nitrophenylcarbonyl)oxy]cyclohex-1-enecarboxylate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of methyl (3S,5R)-5-[(tert-butyldimethylsilyl)oxy]-3-[(p-nitrophenylcarbonyl)oxy]cyclohex-1-enecarboxylate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of methyl (3S,5R)-5-[(tert-butyldimethylsilyl)oxy]-3-[(p-nitrophenylcarbonyl)oxy]cyclohex-1-enecarboxylate

There total 7 articles about methyl (3S,5R)-5-[(tert-butyldimethylsilyl)oxy]-3-[(p-nitrophenylcarbonyl)oxy]cyclohex-1-enecarboxylate 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: 98.0%

: 122-04-3
4-nitro-benzoyl chloride

: 262594-23-0
methyl (3S,5R)-5-[(tert-butyldimethylsilyl)oxy]-3-hydroxy-cyclohex-1-enecarboxylate

: 301153-82-2
methyl (3S,5R)-5-[(tert-butyldimethylsilyl)oxy]-3-[(p-nitrophenylcarbonyl)oxy]cyclohex-1-enecarboxylate

Guidance literature:: With pyridine; at 20 ℃; for 1h;
DOI:10.1021/jo000443l

Reference yield:

: 77-95-2
D-(-)-quinic acid

: 301153-82-2
methyl (3S,5R)-5-[(tert-butyldimethylsilyl)oxy]-3-[(p-nitrophenylcarbonyl)oxy]cyclohex-1-enecarboxylate

Guidance literature:: Multi-step reaction with 7 steps

1: 100 percent / HCl / 6 h / 60 °C

2: 74 percent / Et₃N / dimethylformamide / 16 h / 20 °C

3: 83 percent / CH₂Cl₂ / 120 h / 20 °C

4: 93 percent / Bu₃SnH; AIBN / toluene / 2 h / 85 °C

5: 80 percent / pyridine; POCl₃ / 10 h / 20 °C

6: 84 percent / TBAF / tetrahydrofuran / 15 h / 0 °C

7: 98 percent / pyridine / 1 h / 20 °C

With pyridine; hydrogenchloride; 2,2'-azobis(isobutyronitrile); tetrabutyl ammonium fluoride; tri-n-butyl-tin hydride; triethylamine; trichlorophosphate; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; toluene; 1: Methylation / 2: silylation / 3: thioacylation / 4: dethiocarboxylation / 5: Dehydration / 6: Dehydration / 7: Condensation;
DOI:10.1021/jo000443l

Reference yield:

: 191916-39-9
methyl (-)-quinate

: 301153-82-2
methyl (3S,5R)-5-[(tert-butyldimethylsilyl)oxy]-3-[(p-nitrophenylcarbonyl)oxy]cyclohex-1-enecarboxylate

Guidance literature:: Multi-step reaction with 6 steps

1: 74 percent / Et₃N / dimethylformamide / 16 h / 20 °C

2: 83 percent / CH₂Cl₂ / 120 h / 20 °C

3: 93 percent / Bu₃SnH; AIBN / toluene / 2 h / 85 °C

4: 80 percent / pyridine; POCl₃ / 10 h / 20 °C

5: 84 percent / TBAF / tetrahydrofuran / 15 h / 0 °C

6: 98 percent / pyridine / 1 h / 20 °C

With pyridine; 2,2'-azobis(isobutyronitrile); tetrabutyl ammonium fluoride; tri-n-butyl-tin hydride; triethylamine; trichlorophosphate; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; toluene; 1: silylation / 2: thioacylation / 3: dethiocarboxylation / 4: Dehydration / 5: Dehydration / 6: Condensation;
DOI:10.1021/jo000443l