2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (S)-3-dibenzylamino-4-(2-methoxy-ethoxy)-butyl ester

Base Information

Chemical Name:2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (S)-3-dibenzylamino-4-(2-methoxy-ethoxy)-butyl ester
CAS No.:214832-87-8
Molecular Formula:C₂₉H₄₂N₂O₅
Molecular Weight:498.663
Hs Code.:

Synonyms:2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (S)-3-dibenzylamino-4-(2-methoxy-ethoxy)-butyl ester

Suppliers and Price of 2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (S)-3-dibenzylamino-4-(2-methoxy-ethoxy)-butyl 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 2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (S)-3-dibenzylamino-4-(2-methoxy-ethoxy)-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (S)-3-dibenzylamino-4-(2-methoxy-ethoxy)-butyl ester

There total 4 articles about 2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (S)-3-dibenzylamino-4-(2-methoxy-ethoxy)-butyl 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: 88.0%

: 146176-60-5
2,2,4,4-tetramethyl-1,3-oxazolidine-3-carbonyl chloride

: 214832-95-8
(S)-3-Dibenzylamino-4-(2-methoxy-ethoxy)-butan-1-ol

: 214832-87-8
2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (S)-3-dibenzylamino-4-(2-methoxy-ethoxy)-butyl ester

Guidance literature:: With sodium hydride; In tetrahydrofuran; 1.) r.t., 3 h, 2.) 65 deg C, 16 h;
DOI:10.1055/s-1998-6100

Reference yield:

: 137428-32-1
(2S)-2-[bis(phenylmethyl)amino]-1,4-butanediol

: 214832-87-8
2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (S)-3-dibenzylamino-4-(2-methoxy-ethoxy)-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 55 percent / Et₃N, DMAP / CH₂Cl₂ / 8 h / 40 °C

2: 44 percent / NaH, Bu₄NI, DMAP / tetrahydrofuran / 1.) r.t., 4 h, 2.) 65 deg C, 20 h

3: 99 percent / TBAF / tetrahydrofuran; diethyl ether / 14 h / Ambient temperature

4: 88 percent / NaH / tetrahydrofuran / 1.) r.t., 3 h, 2.) 65 deg C, 16 h

With dmap; tetrabutyl ammonium fluoride; tetra-(n-butyl)ammonium iodide; sodium hydride; triethylamine; In tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1055/s-1998-6100

Reference yield:

: 152299-13-3
(2S)-4-{[tert-butyl(dimethyl)silyl]oxy}-2-(dibenzylamino)butan-1-ol

: 214832-87-8
2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (S)-3-dibenzylamino-4-(2-methoxy-ethoxy)-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 44 percent / NaH, Bu₄NI, DMAP / tetrahydrofuran / 1.) r.t., 4 h, 2.) 65 deg C, 20 h

2: 99 percent / TBAF / tetrahydrofuran; diethyl ether / 14 h / Ambient temperature

3: 88 percent / NaH / tetrahydrofuran / 1.) r.t., 3 h, 2.) 65 deg C, 16 h

With dmap; tetrabutyl ammonium fluoride; tetra-(n-butyl)ammonium iodide; sodium hydride; In tetrahydrofuran; diethyl ether;
DOI:10.1055/s-1998-6100