(2S,3R,4S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-2-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:(2S,3R,4S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-2-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester
CAS No.:294659-37-3
Molecular Formula:C₅₉H₆₇NO₁₀
Molecular Weight:950.182
Hs Code.:

(2S,3R,4S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-2-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester

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Chemical Property of (2S,3R,4S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-2-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester

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Technology Process of (2S,3R,4S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-2-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester

There total 6 articles about (2S,3R,4S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-2-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethyl)-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: 83.0%

: 100-39-0
benzyl bromide

: 294659-39-5
(2S,3R,4S)-3,4-Dihydroxy-2-hydroxymethyl-2-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester

: 294659-37-3
(2S,3R,4S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-2-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: With potassium hydroxide;
DOI:10.1080/07328300008544107

Reference yield:

: 85716-43-4
methyl 6-deoxy-6-iodo-2,3,4-tri-O-benzyl-α-D-glucopyranoside

: 294659-37-3
(2S,3R,4S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-2-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: tetrahydrofuran / -78 °C

2: 91 percent / OsO₄ / acetone

3: 71 percent / LiAlH₄ / diethyl ether

4: 83 percent / KOH

With potassium hydroxide; osmium(VIII) oxide; lithium aluminium tetrahydride; In tetrahydrofuran; diethyl ether; acetone; 1: Alkylation / 2: cis-dihydroxylation / 3: Reduction / 4: Etherification;
DOI:10.1080/07328300008544107

Reference yield:

: 202477-57-4
1-(tert-butoxycarbonyl)-2,5-dihydro-1H-pyrrole-2-carboxylic acid methyl ester

: 294659-37-3
(2S,3R,4S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-2-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: tetrahydrofuran / -78 °C

2: 91 percent / OsO₄ / acetone

3: 71 percent / LiAlH₄ / diethyl ether

4: 83 percent / KOH

With potassium hydroxide; osmium(VIII) oxide; lithium aluminium tetrahydride; In tetrahydrofuran; diethyl ether; acetone; 1: Alkylation / 2: cis-dihydroxylation / 3: Reduction / 4: Etherification;
DOI:10.1080/07328300008544107