[(2R,6R)-4-((R)-2-Hydroxy-1-phenyl-ethyl)-3-oxo-6-phenyl-morpholin-2-yl]-acetic acid tert-butyl ester

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Chemical Name:[(2R,6R)-4-((R)-2-Hydroxy-1-phenyl-ethyl)-3-oxo-6-phenyl-morpholin-2-yl]-acetic acid tert-butyl ester
CAS No.:250596-73-7
Molecular Formula:C₂₄H₂₉NO₅
Molecular Weight:411.498
Hs Code.:

Synonyms:[(2R,6R)-4-((R)-2-Hydroxy-1-phenyl-ethyl)-3-oxo-6-phenyl-morpholin-2-yl]-acetic acid tert-butyl ester

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Chemical Property of [(2R,6R)-4-((R)-2-Hydroxy-1-phenyl-ethyl)-3-oxo-6-phenyl-morpholin-2-yl]-acetic acid tert-butyl ester

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Technology Process of [(2R,6R)-4-((R)-2-Hydroxy-1-phenyl-ethyl)-3-oxo-6-phenyl-morpholin-2-yl]-acetic acid tert-butyl ester

There total 6 articles about [(2R,6R)-4-((R)-2-Hydroxy-1-phenyl-ethyl)-3-oxo-6-phenyl-morpholin-2-yl]-acetic acid tert-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: 76.0%

: 5292-43-3
bromoacetic acid tert-butyl ester

: 250596-67-9
(R)-4-((R)-2-Hydroxy-1-phenyl-ethyl)-6-phenyl-morpholin-3-one

: 250596-73-7
[(2R,6R)-4-((R)-2-Hydroxy-1-phenyl-ethyl)-3-oxo-6-phenyl-morpholin-2-yl]-acetic acid tert-butyl ester

Guidance literature:: (R)-4-((R)-2-Hydroxy-1-phenyl-ethyl)-6-phenyl-morpholin-3-one; With N,N,N,N,N,N-hexamethylphosphoric triamide; sec.-butyllithium; In tetrahydrofuran; at -78 ℃; for 0.5h;

bromoacetic acid tert-butyl ester; In tetrahydrofuran; at -78 ℃;
DOI:10.1016/S0040-4039(99)01530-0

Reference yield:

: 20780-53-4
(R)-Styrene oxide

: 250596-73-7
[(2R,6R)-4-((R)-2-Hydroxy-1-phenyl-ethyl)-3-oxo-6-phenyl-morpholin-2-yl]-acetic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: methanol / 10 h / 40 °C

2.1: aq. NaOH / tetrahydrofuran / 2 h

3.1: NaH / tetrahydrofuran / 10 h

4.1: TBAF / tetrahydrofuran / 2 h / 20 °C

5.1: sec-BuLi; HMPA / tetrahydrofuran / 0.5 h / -78 °C

5.2: 76 percent / tetrahydrofuran / -78 °C

With N,N,N,N,N,N-hexamethylphosphoric triamide; sodium hydroxide; tetrabutyl ammonium fluoride; sec.-butyllithium; sodium hydride; In tetrahydrofuran; methanol; 1.1: Alkylation / 2.1: Acylation / 3.1: Cyclization / 4.1: desilylation / 5.1: Metallation / 5.2: Alkylation;
DOI:10.1016/S0040-4039(99)01530-0

Reference yield:

: 120417-13-2,120666-55-9
(1R)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-phenylethanamine

: 250596-73-7
[(2R,6R)-4-((R)-2-Hydroxy-1-phenyl-ethyl)-3-oxo-6-phenyl-morpholin-2-yl]-acetic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: methanol / 10 h / 40 °C

2.1: aq. NaOH / tetrahydrofuran / 2 h

3.1: NaH / tetrahydrofuran / 10 h

4.1: TBAF / tetrahydrofuran / 2 h / 20 °C

5.1: sec-BuLi; HMPA / tetrahydrofuran / 0.5 h / -78 °C

5.2: 76 percent / tetrahydrofuran / -78 °C

With N,N,N,N,N,N-hexamethylphosphoric triamide; sodium hydroxide; tetrabutyl ammonium fluoride; sec.-butyllithium; sodium hydride; In tetrahydrofuran; methanol; 1.1: Alkylation / 2.1: Acylation / 3.1: Cyclization / 4.1: desilylation / 5.1: Metallation / 5.2: Alkylation;
DOI:10.1016/S0040-4039(99)01530-0