2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (R)-2-dibenzylamino-butyl ester

Base Information

Chemical Name:2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (R)-2-dibenzylamino-butyl ester
CAS No.:247576-09-6
Molecular Formula:C₂₆H₃₆N₂O₃
Molecular Weight:424.583
Hs Code.:

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

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Chemical Property of 2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (R)-2-dibenzylamino-butyl ester

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

There total 2 articles about 2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (R)-2-dibenzylamino-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: 79.0%

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

: 249922-61-0
(2R)-N,N-dibenzyl-2-aminobutan-1-ol

: 247576-09-6
2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (R)-2-dibenzylamino-butyl ester

Guidance literature:: (2R)-N,N-dibenzyl-2-aminobutan-1-ol; With sodium hydride; In tetrahydrofuran; for 1h; Heating;

2,2,4,4-tetramethyl-1,3-oxazolidine-3-carbonyl chloride; In tetrahydrofuran; for 6h; Heating;
DOI:10.1055/s-1999-3575

Reference yield:

: 100-39-0
benzyl bromide

: 247576-09-6
2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (R)-2-dibenzylamino-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

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

1.2: 98 percent / aq. methanol / 6 h / Heating

2.1: NaH / tetrahydrofuran / 1 h / Heating

2.2: 79 percent / tetrahydrofuran / 6 h / Heating

With sodium hydroxide; sodium hydride; potassium carbonate; In tetrahydrofuran; methanol; 1.1: Metallation / 1.2: Alkylation / 2.1: Metallation / 2.2: Acylation;
DOI:10.1055/s-1999-3575

Reference yield: 86.0%

: 120205-96-1,121010-18-2,129286-74-4,111060-63-0
(S)-2-(dibenzylamino)propanal

: 247576-09-6
2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (R)-2-dibenzylamino-butyl ester

: 247576-07-4
(2S,3S,4R,5R)-2,5-Bis(N,N-dibenzylamino)-4-O-(2,2,4,4-tetramethyl-1,3-oxazolidine-3-carbonyl)-3,4-heptanediol

Guidance literature:: 2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (R)-2-dibenzylamino-butyl ester; With N,N,N,N,-tetramethylethylenediamine; sec.-butyllithium; In diethyl ether; hexane; cyclohexane; at -78 ℃; for 6h;

(S)-2-(dibenzylamino)propanal; In diethyl ether; hexane; cyclohexane; at -78 - 20 ℃; for 12h;
DOI:10.1055/s-1999-3576