(2S,3S)-3-Benzyl-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester 2-tert-butyl ester

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Chemical Name:(2S,3S)-3-Benzyl-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester 2-tert-butyl ester
CAS No.:745016-64-2
Molecular Formula:C₂₄H₂₉NO₄
Molecular Weight:395.499
Hs Code.:

Synonyms:(2S,3S)-3-Benzyl-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester 2-tert-butyl ester

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Chemical Property of (2S,3S)-3-Benzyl-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester 2-tert-butyl ester

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Technology Process of (2S,3S)-3-Benzyl-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester 2-tert-butyl ester

There total 5 articles about (2S,3S)-3-Benzyl-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester 2-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:

: 41979-02-6
α-lithiobenzyl phenyl sulfide

: 745016-64-2
(2S,3S)-3-Benzyl-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester 2-tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: BuLi; TMEDA / -78 °C

1.2: water; Ra-Ni / acetone / 12 h / Heating

2.1: HCl / ethyl acetate / -20 °C

3.1: LAH / tetrahydrofuran / Heating

4.1: aq. K₂CO₃ / tetrahydrofuran

5.1: acetone; Jones reagent

6.1: H₂SO₄ / CH₂Cl₂

With hydrogenchloride; lithium aluminium tetrahydride; n-butyllithium; jones reagent; N,N,N,N,-tetramethylethylenediamine; sulfuric acid; potassium carbonate; acetone; In tetrahydrofuran; dichloromethane; ethyl acetate; 5.1: Jones oxidation;
DOI:10.1016/j.bmcl.2004.01.078

Reference yield:

: 81658-27-7
(S)-tert-butyl 2-(((tert-butyldimethylsilyl)oxy)methyl)-5-oxo-2,5-dihydro-1H-pyrrole-1-carboxylate

: 745016-64-2
(2S,3S)-3-Benzyl-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester 2-tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: BuLi; TMEDA / -78 °C

1.2: water; Ra-Ni / acetone / 12 h / Heating

2.1: HCl / ethyl acetate / -20 °C

3.1: LAH / tetrahydrofuran / Heating

4.1: aq. K₂CO₃ / tetrahydrofuran

5.1: acetone; Jones reagent

6.1: H₂SO₄ / CH₂Cl₂

With hydrogenchloride; lithium aluminium tetrahydride; n-butyllithium; jones reagent; N,N,N,N,-tetramethylethylenediamine; sulfuric acid; potassium carbonate; acetone; In tetrahydrofuran; dichloromethane; ethyl acetate; 5.1: Jones oxidation;
DOI:10.1016/j.bmcl.2004.01.078

Reference yield:

: 696645-92-8
((2S,3S)-3-Benzyl-pyrrolidin-2-yl)-methanol

: 745016-64-2
(2S,3S)-3-Benzyl-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester 2-tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: aq. K₂CO₃ / tetrahydrofuran

2: acetone; Jones reagent

3: H₂SO₄ / CH₂Cl₂

With jones reagent; sulfuric acid; potassium carbonate; acetone; In tetrahydrofuran; dichloromethane; 2: Jones oxidation;
DOI:10.1016/j.bmcl.2004.01.078