(R)-1-(4-Methoxy-benzyl)-4-methyl-4-methylsulfanyl-3,5-dioxo-pyrrolidine-2-carboxylic acid methyl ester

Base Information

Chemical Name:(R)-1-(4-Methoxy-benzyl)-4-methyl-4-methylsulfanyl-3,5-dioxo-pyrrolidine-2-carboxylic acid methyl ester
CAS No.:212772-59-3
Molecular Formula:C₁₆H₁₉NO₅S
Molecular Weight:337.397
Hs Code.:

Synonyms:(R)-1-(4-Methoxy-benzyl)-4-methyl-4-methylsulfanyl-3,5-dioxo-pyrrolidine-2-carboxylic acid methyl ester

Suppliers and Price of (R)-1-(4-Methoxy-benzyl)-4-methyl-4-methylsulfanyl-3,5-dioxo-pyrrolidine-2-carboxylic 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 1 raw suppliers

Chemical Property of (R)-1-(4-Methoxy-benzyl)-4-methyl-4-methylsulfanyl-3,5-dioxo-pyrrolidine-2-carboxylic acid methyl ester

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (R)-1-(4-Methoxy-benzyl)-4-methyl-4-methylsulfanyl-3,5-dioxo-pyrrolidine-2-carboxylic acid methyl ester

There total 4 articles about (R)-1-(4-Methoxy-benzyl)-4-methyl-4-methylsulfanyl-3,5-dioxo-pyrrolidine-2-carboxylic 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: 93.0%

: N-(4-Methoxy-benzyl)-N-methoxycarbonylmethyl-2-methyl-2-methylsulfanyl-malonamic acid methyl ester

: 212772-59-3
(R)-1-(4-Methoxy-benzyl)-4-methyl-4-methylsulfanyl-3,5-dioxo-pyrrolidine-2-carboxylic acid methyl ester

Guidance literature:: With lithium diisopropyl amide; In tetrahydrofuran; at -78 ℃; for 2h;
DOI:10.1002/(SICI)1521-3773(19980703)37:12<1676::AID-ANIE1676>3.0.CO;2-T

Reference yield:

: 20839-80-9
(4-methoxybenzylamino)acetic acid methyl ester

: 212772-59-3
(R)-1-(4-Methoxy-benzyl)-4-methyl-4-methylsulfanyl-3,5-dioxo-pyrrolidine-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / CH₂Cl₂ / 1 h / 23 °C

2: 93 percent / LDA / tetrahydrofuran / 2 h / -78 °C

With triethylamine; lithium diisopropyl amide; In tetrahydrofuran; dichloromethane;
DOI:10.1002/(SICI)1521-3773(19980703)37:12<1676::AID-ANIE1676>3.0.CO;2-T

Reference yield:

: 2-Chlorocarbonyl-2-methylsulfanyl-propionic acid methyl ester

: 212772-59-3
(R)-1-(4-Methoxy-benzyl)-4-methyl-4-methylsulfanyl-3,5-dioxo-pyrrolidine-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / CH₂Cl₂ / 1 h / 23 °C

2: 93 percent / LDA / tetrahydrofuran / 2 h / -78 °C

With triethylamine; lithium diisopropyl amide; In tetrahydrofuran; dichloromethane;
DOI:10.1002/(SICI)1521-3773(19980703)37:12<1676::AID-ANIE1676>3.0.CO;2-T