(2S,3R,4R,5S)-3,4-Bis-benzyloxy-2,5-bis-(4-methoxy-benzyloxymethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:(2S,3R,4R,5S)-3,4-Bis-benzyloxy-2,5-bis-(4-methoxy-benzyloxymethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester
CAS No.:419564-87-7
Molecular Formula:C₄₁H₄₉NO₈
Molecular Weight:683.842
Hs Code.:

Synonyms:(2S,3R,4R,5S)-3,4-Bis-benzyloxy-2,5-bis-(4-methoxy-benzyloxymethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester

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Chemical Property of (2S,3R,4R,5S)-3,4-Bis-benzyloxy-2,5-bis-(4-methoxy-benzyloxymethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester

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Technology Process of (2S,3R,4R,5S)-3,4-Bis-benzyloxy-2,5-bis-(4-methoxy-benzyloxymethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester

There total 7 articles about (2S,3R,4R,5S)-3,4-Bis-benzyloxy-2,5-bis-(4-methoxy-benzyloxymethyl)-pyrrolidine-1-carboxylic 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: 98.0%

: 100-39-0
benzyl bromide

: 419564-84-4
(2S,3R,4R,5S)-3,4-Dihydroxy-2,5-bis-(4-methoxy-benzyloxymethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester

: 419564-87-7
(2S,3R,4R,5S)-3,4-Bis-benzyloxy-2,5-bis-(4-methoxy-benzyloxymethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: With sodium hydride; In tetrahydrofuran; at 0 - 20 ℃; for 12h;
DOI:10.1021/jo010937y

Reference yield:

: 201536-29-0
1,3(R):4,6(R)-bis-O-(4-methoxybenzylidene)-D-mannitol

: 419564-87-7
(2S,3R,4R,5S)-3,4-Bis-benzyloxy-2,5-bis-(4-methoxy-benzyloxymethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: Et₃N / CH₂Cl₂; dimethylformamide / 0.5 h / 0 °C

2: 7.25 g / 6 h / 130 °C

3: 60 percent / LiAlH₄; AlCl₃ / diethyl ether / 1.5 h / Heating

4: H₂ / 20percent Pd(OH₂) on C / methanol / 4 h

5: 3.5 g / methanol / 20 °C

6: 98 percent / NaH / tetrahydrofuran / 12 h / 0 - 20 °C

With lithium aluminium tetrahydride; aluminium trichloride; hydrogen; sodium hydride; triethylamine; 20percent Pd(OH₂) on C; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo010937y

Reference yield:

: 419564-82-2
(4aS,5aS,9aR,9bR)-5-Benzyl-2,8-bis-(4-methoxy-phenyl)-hexahydro-bis[1,3]dioxino[5,4-b;4',5'-d]pyrrole

: 419564-87-7
(2S,3R,4R,5S)-3,4-Bis-benzyloxy-2,5-bis-(4-methoxy-benzyloxymethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 60 percent / LiAlH₄; AlCl₃ / diethyl ether / 1.5 h / Heating

2: H₂ / 20percent Pd(OH₂) on C / methanol / 4 h

3: 3.5 g / methanol / 20 °C

4: 98 percent / NaH / tetrahydrofuran / 12 h / 0 - 20 °C

With lithium aluminium tetrahydride; aluminium trichloride; hydrogen; sodium hydride; 20percent Pd(OH₂) on C; In tetrahydrofuran; methanol; diethyl ether;
DOI:10.1021/jo010937y