2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (1S,2R)-2-dibenzylamino-1-methyl-2-phenyl-ethyl ester

Base Information

Chemical Name:2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (1S,2R)-2-dibenzylamino-1-methyl-2-phenyl-ethyl ester
CAS No.:249923-04-4
Molecular Formula:C₃₁H₃₈N₂O₃
Molecular Weight:486.654
Hs Code.:

Synonyms:2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (1S,2R)-2-dibenzylamino-1-methyl-2-phenyl-ethyl ester

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Chemical Property of 2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (1S,2R)-2-dibenzylamino-1-methyl-2-phenyl-ethyl ester

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Technology Process of 2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (1S,2R)-2-dibenzylamino-1-methyl-2-phenyl-ethyl ester

There total 4 articles about 2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (1S,2R)-2-dibenzylamino-1-methyl-2-phenyl-ethyl 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: 71.0%

: 249922-64-3
2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (R)-2-dibenzylamino-2-phenyl-ethyl ester

: 74-88-4
methyl iodide

: 249923-04-4
2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (1S,2R)-2-dibenzylamino-1-methyl-2-phenyl-ethyl ester

Guidance literature:: 2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (R)-2-dibenzylamino-2-phenyl-ethyl ester; With sec.-butyllithium; (-)-sparteine; In diethyl ether; hexane; cyclohexane; at -78 ℃;

methyl iodide; In diethyl ether; hexane; cyclohexane; at -78 - 20 ℃; for 12h;
DOI:10.1055/s-1999-3575

Reference yield:

: 193476-02-7
(+)-(2R)-2-[bis(phenylmethyl)amino]-2-phenylethanol

: 249923-04-4
2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (1S,2R)-2-dibenzylamino-1-methyl-2-phenyl-ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: NaH / tetrahydrofuran / 1 h / Heating

1.2: 94 percent / DMPU / tetrahydrofuran / 6 h / Heating

2.1: s-BuLi; (-)-sparteine / diethyl ether; cyclohexane; hexane / -78 °C

2.2: 71 percent / diethyl ether; cyclohexane; hexane / 12 h / -78 - 20 °C

With sec.-butyllithium; sodium hydride; (-)-sparteine; In tetrahydrofuran; diethyl ether; hexane; cyclohexane; 1.1: Metallation / 1.2: Acylation / 2.1: Metallation / 2.2: Methylation;
DOI:10.1055/s-1999-3575

Reference yield:

: 56613-80-0
D-2-phenylglycinol

: 249923-04-4
2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (1S,2R)-2-dibenzylamino-1-methyl-2-phenyl-ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: K₂CO₃; NaOH / aq. methanol / 0.5 h / Heating

1.2: 46 percent / aq. methanol / 6 h / Heating

2.1: NaH / tetrahydrofuran / 1 h / Heating

2.2: 94 percent / DMPU / tetrahydrofuran / 6 h / Heating

3.1: s-BuLi; (-)-sparteine / diethyl ether; cyclohexane; hexane / -78 °C

3.2: 71 percent / diethyl ether; cyclohexane; hexane / 12 h / -78 - 20 °C

With sodium hydroxide; sec.-butyllithium; sodium hydride; potassium carbonate; (-)-sparteine; In tetrahydrofuran; methanol; diethyl ether; hexane; cyclohexane; 1.1: Metallation / 1.2: Alkylation / 2.1: Metallation / 2.2: Acylation / 3.1: Metallation / 3.2: Methylation;
DOI:10.1055/s-1999-3575