4-(5,5-Dimethyl-6-oxo-cyclohex-1-enyl)-3-formyl-butyric acid methyl ester

Base Information

Chemical Name:4-(5,5-Dimethyl-6-oxo-cyclohex-1-enyl)-3-formyl-butyric acid methyl ester
CAS No.:113522-82-0
Molecular Formula:C₁₄H₂₀O₄
Molecular Weight:252.31
Hs Code.:

Synonyms:4-(5,5-Dimethyl-6-oxo-cyclohex-1-enyl)-3-formyl-butyric acid methyl ester

Suppliers and Price of 4-(5,5-Dimethyl-6-oxo-cyclohex-1-enyl)-3-formyl-butyric acid methyl ester

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 4-(5,5-Dimethyl-6-oxo-cyclohex-1-enyl)-3-formyl-butyric acid methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 4-(5,5-Dimethyl-6-oxo-cyclohex-1-enyl)-3-formyl-butyric acid methyl ester

There total 10 articles about 4-(5,5-Dimethyl-6-oxo-cyclohex-1-enyl)-3-formyl-butyric acid methyl ester 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: 75.0%

: 113522-71-7
4-(5,5-Dimethyl-6-oxo-cyclohex-1-enyl)-3-hydroxymethyl-butyric acid methyl ester

: 113522-82-0
4-(5,5-Dimethyl-6-oxo-cyclohex-1-enyl)-3-formyl-butyric acid methyl ester

Guidance literature:: With oxalyl dichloride; dimethyl sulfoxide; In dichloromethane; at -55 ℃; for 0.25h;
DOI:10.1016/S0040-4039(00)96293-2

Reference yield:

: 77661-80-4
2-(2-(benzyloxy)ethyl)propane-1,3-diol

: 113522-82-0
4-(5,5-Dimethyl-6-oxo-cyclohex-1-enyl)-3-formyl-butyric acid methyl ester

Guidance literature:: Multi-step reaction with 9 steps

1: 92 percent / Bu₂SnO (stannylene acetal) Bu₄NBr / toluene / 18 h / Heating

2: 92 percent / Ph₃P, imidazole, I₂ / tetrahydrofuran / 1 h / 20 °C

3: 2.) p-TsOH / 1.) THF, -78 deg C to 20 deg C, 5h; 2.) 5h, 20 deg C

4: Et₃N / methanol / 12 h / 20 °C

5: 71 percent / boron tribromide / CH₂Cl₂ / 0.25 h / 0 °C

6: Jones reagent / acetone / 1 h / 20 °C

7: Bu₄NF / tetrahydrofuran / 8 h / 20 °C

8: diethyl ether; methanol / 20 °C

9: 75 percent / (COCl)2 DMSO / CH₂Cl₂ / 0.25 h / -55 °C

With 1H-imidazole; jones reagent; oxalyl dichloride; Bu₂SnO (stannylene acetal) Bu₄NBr; tetrabutyl ammonium fluoride; iodine; boron tribromide; toluene-4-sulfonic acid; dimethyl sulfoxide; triethylamine; triphenylphosphine; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; acetone; toluene;
DOI:10.1016/S0040-4039(00)96293-2

Reference yield:

: 113522-70-6
4-(5,5-Dimethyl-6-oxo-cyclohex-1-enyl)-3-hydroxymethyl-butyric acid

: 113522-82-0
4-(5,5-Dimethyl-6-oxo-cyclohex-1-enyl)-3-formyl-butyric acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: diethyl ether; methanol / 20 °C

2: 75 percent / (COCl)2 DMSO / CH₂Cl₂ / 0.25 h / -55 °C

With oxalyl dichloride; dimethyl sulfoxide; In methanol; diethyl ether; dichloromethane;
DOI:10.1016/S0040-4039(00)96293-2