(1R,2R)-1,2-diphenyl-2-(4-trifluoromethylbenzyloxy)ethyl phenylglyoxylate

Base Information

Chemical Name:(1R,2R)-1,2-diphenyl-2-(4-trifluoromethylbenzyloxy)ethyl phenylglyoxylate
CAS No.:415920-05-7
Molecular Formula:C₃₀H₂₃F₃O₄
Molecular Weight:504.505
Hs Code.:

Synonyms:(1R,2R)-1,2-diphenyl-2-(4-trifluoromethylbenzyloxy)ethyl phenylglyoxylate

Suppliers and Price of (1R,2R)-1,2-diphenyl-2-(4-trifluoromethylbenzyloxy)ethyl phenylglyoxylate

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 (1R,2R)-1,2-diphenyl-2-(4-trifluoromethylbenzyloxy)ethyl phenylglyoxylate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (1R,2R)-1,2-diphenyl-2-(4-trifluoromethylbenzyloxy)ethyl phenylglyoxylate

There total 4 articles about (1R,2R)-1,2-diphenyl-2-(4-trifluoromethylbenzyloxy)ethyl phenylglyoxylate 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: 99.0%

: 611-73-4
Benzoylformic acid

: 415919-99-2
(1R,2R)-1,2-diphenyl-2-(4-trifluoromethylbenzyloxy)ethanol

: 415920-05-7
(1R,2R)-1,2-diphenyl-2-(4-trifluoromethylbenzyloxy)ethyl phenylglyoxylate

Guidance literature:: With dmap; dicyclohexyl-carbodiimide; In dichloromethane; at 0 - 25 ℃;
DOI:10.1016/S0040-4020(01)01117-6

Reference yield:

: 455-19-6
4-Trifluoromethylbenzaldehyde

: 415920-05-7
(1R,2R)-1,2-diphenyl-2-(4-trifluoromethylbenzyloxy)ethyl phenylglyoxylate

Guidance literature:: Multi-step reaction with 3 steps

1: 77 percent / p-toluenesulfonic acid / benzene / Heating

2: 84 percent / DIBAL / toluene / 0 °C

3: 99 percent / 4-(N,N-dimethylamino)pyridine; DCC / CH₂Cl₂ / 0 - 25 °C

With dmap; diisobutylaluminium hydride; toluene-4-sulfonic acid; dicyclohexyl-carbodiimide; In dichloromethane; toluene; benzene;
DOI:10.1016/S0040-4020(01)01117-6

Reference yield:

: 52340-78-0
(R,R)-hydroxybenzoin

: 415920-05-7
(1R,2R)-1,2-diphenyl-2-(4-trifluoromethylbenzyloxy)ethyl phenylglyoxylate

Guidance literature:: Multi-step reaction with 3 steps

1: 77 percent / p-toluenesulfonic acid / benzene / Heating

2: 84 percent / DIBAL / toluene / 0 °C

3: 99 percent / 4-(N,N-dimethylamino)pyridine; DCC / CH₂Cl₂ / 0 - 25 °C

With dmap; diisobutylaluminium hydride; toluene-4-sulfonic acid; dicyclohexyl-carbodiimide; In dichloromethane; toluene; benzene;
DOI:10.1016/S0040-4020(01)01117-6