(2R)-2-[3-(1,3-dioxolan-2-yl)prop-1-yl]-1-(4-methylphenylsulfonyl)pyrrolidin-3-one

Base Information

Chemical Name:(2R)-2-[3-(1,3-dioxolan-2-yl)prop-1-yl]-1-(4-methylphenylsulfonyl)pyrrolidin-3-one
CAS No.:866141-90-4
Molecular Formula:C₁₇H₂₃NO₅S
Molecular Weight:353.439
Hs Code.:

Synonyms:(2R)-2-[3-(1,3-dioxolan-2-yl)prop-1-yl]-1-(4-methylphenylsulfonyl)pyrrolidin-3-one

Suppliers and Price of (2R)-2-[3-(1,3-dioxolan-2-yl)prop-1-yl]-1-(4-methylphenylsulfonyl)pyrrolidin-3-one

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 (2R)-2-[3-(1,3-dioxolan-2-yl)prop-1-yl]-1-(4-methylphenylsulfonyl)pyrrolidin-3-one

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2R)-2-[3-(1,3-dioxolan-2-yl)prop-1-yl]-1-(4-methylphenylsulfonyl)pyrrolidin-3-one

There total 8 articles about (2R)-2-[3-(1,3-dioxolan-2-yl)prop-1-yl]-1-(4-methylphenylsulfonyl)pyrrolidin-3-one 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: 81.0%

: 866141-92-6
(2R,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-(3-[1,3]dioxolan-2-yl-propyl)-1-(toluene-4-sulfonyl)-pyrrolidine

: 866141-90-4
(2R)-2-[3-(1,3-dioxolan-2-yl)prop-1-yl]-1-(4-methylphenylsulfonyl)pyrrolidin-3-one

Guidance literature:: (2R,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-(3-[1,3]dioxolan-2-yl-propyl)-1-(toluene-4-sulfonyl)-pyrrolidine; With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 1h;

With Celite; pyridinium chlorochromate; In dichloromethane; at 20 ℃; for 10h;
DOI:10.3987/COM-05-10470

Reference yield:

: 1063998-64-0
(2S,4R)-4-Hydroxy-pyrrolidine-2-carbonyl chloride

: 866141-90-4
(2R)-2-[3-(1,3-dioxolan-2-yl)prop-1-yl]-1-(4-methylphenylsulfonyl)pyrrolidin-3-one

Guidance literature:: Multi-step reaction with 6 steps

1.1: triethylamine / CH₂Cl₂

2.1: imidazole / dimethylformamide

3.1: sodium borohydride; lithium chloride / methanol

4.1: oxalyl chloride; dimethyl sulfoxide / CH₂Cl₂; triethylamine / -78 - 20 °C

4.2: 75 percent / n-butyllithium / tetrahydrofuran; hexane / -78 - 8 °C

5.1: 90 percent / H₂ / Pd/C / ethyl acetate / 10 h / 20 °C

6.1: n-tetrabutylammonium fluoride / tetrahydrofuran / 1 h / 20 °C

6.2: 81 percent / pyridinium chlorochromate; Celite / CH₂Cl₂ / 10 h / 20 °C

With 1H-imidazole; sodium tetrahydroborate; oxalyl dichloride; tetrabutyl ammonium fluoride; hydrogen; dimethyl sulfoxide; triethylamine; lithium chloride; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate; triethylamine; N,N-dimethyl-formamide; 4.1: Swern oxidation;
DOI:10.3987/COM-05-10470

Reference yield:

: (2S,4R)-4-Hydroxy-1-(toluene-4-sulfonyl)-pyrrolidine-2-carbonyl chloride

: 866141-90-4
(2R)-2-[3-(1,3-dioxolan-2-yl)prop-1-yl]-1-(4-methylphenylsulfonyl)pyrrolidin-3-one

Guidance literature:: Multi-step reaction with 5 steps

1.1: imidazole / dimethylformamide

2.1: sodium borohydride; lithium chloride / methanol

3.1: oxalyl chloride; dimethyl sulfoxide / CH₂Cl₂; triethylamine / -78 - 20 °C

3.2: 75 percent / n-butyllithium / tetrahydrofuran; hexane / -78 - 8 °C

4.1: 90 percent / H₂ / Pd/C / ethyl acetate / 10 h / 20 °C

5.1: n-tetrabutylammonium fluoride / tetrahydrofuran / 1 h / 20 °C

5.2: 81 percent / pyridinium chlorochromate; Celite / CH₂Cl₂ / 10 h / 20 °C

With 1H-imidazole; sodium tetrahydroborate; oxalyl dichloride; tetrabutyl ammonium fluoride; hydrogen; dimethyl sulfoxide; lithium chloride; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate; triethylamine; N,N-dimethyl-formamide; 3.1: Swern oxidation;
DOI:10.3987/COM-05-10470