(2S,4R)-benzyl 4-(tosyloxy)-2-((tosyloxy)methyl)pyrrolidine-1-carboxylate

Base Information

Chemical Name:(2S,4R)-benzyl 4-(tosyloxy)-2-((tosyloxy)methyl)pyrrolidine-1-carboxylate
CAS No.:95687-42-6
Molecular Formula:C₂₇H₂₉NO₈S₂
Molecular Weight:559.661
Hs Code.:
DSSTox Substance ID:DTXSID701104830

Synonyms:SCHEMBL9587450;AKRRZBQIGJJBFF-BJKOFHAPSA-N;DTXSID701104830;(2S,4R)-benzyl 4-(tosyloxy)-2-((tosyloxy)methyl)pyrrolidine-1-carboxylate;AKOS000278397;95687-42-6;(2S,4R)-1-(Carbobenzyloxy)-2-(4-toluenesulfonyloxymeth- yl)-4-(4-toluenesulfonyloxy)-pyrrolidine;(2S,4R)-1-(Carbobenzyloxy)-2-(4-toluenesulfonyloxymethyl)-4-(4-toluenesulfonyloxy)-pyrrolidine;(2S,4R)-1-(carbobenzyloxy)-2-(p-toluenesulfonyloxymeth- yl)-4-(4-toluenesulfonyloxy)-pyrrolidine;(2S,4R)-1-(carbobenzyloxy)-2-(p-toluenesulfonyloxymethyl)-4-(4-toluenesulfonyloxy)-pyrrolidine;Phenylmethyl (2S,4R)-4-[[(4-methylphenyl)sulfonyl]oxy]-2-[[[(4-methylphenyl)sulfonyl]oxy]methyl]-1-pyrrolidinecarboxylate

Suppliers and Price of (2S,4R)-benzyl 4-(tosyloxy)-2-((tosyloxy)methyl)pyrrolidine-1-carboxylate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (2S,4R)-benzyl 4-(tosyloxy)-2-((tosyloxy)methyl)pyrrolidine-1-carboxylate

Chemical Property:

XLogP3:4.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:10
Exact Mass:559.13345923
Heavy Atom Count:38
Complexity:968

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)OCC2CC(CN2C(=O)OCC3=CC=CC=C3)OS(=O)(=O)C4=CC=C(C=C4)C
Isomeric SMILES:CC1=CC=C(C=C1)S(=O)(=O)OC[C@@H]2C[C@H](CN2C(=O)OCC3=CC=CC=C3)OS(=O)(=O)C4=CC=C(C=C4)C

Technology Process of (2S,4R)-benzyl 4-(tosyloxy)-2-((tosyloxy)methyl)pyrrolidine-1-carboxylate

There total 3 articles about (2S,4R)-benzyl 4-(tosyloxy)-2-((tosyloxy)methyl)pyrrolidine-1-carboxylate 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: 82.0%

: 98-59-9
p-toluenesulfonyl chloride

: 1448706-36-2
(2R,4S)-2-hydroxymethyl-4-hydroxy-N-(carbobenzyloxy)pyrrolidine

: 95687-42-6
(2S,4R)-benzyl 4-(tosyloxy)-2-((tosyloxy)methyl)pyrrolidine-1-carboxylate

Guidance literature:: In pyridine;

Reference yield:

: 95687-41-5,1448706-36-2
(2S,4R)-N1-(benzyloxycarbonyl)-4-hydroxy-2-(hydroxymethyl)-pyrrolidine

: 98-59-9
p-toluenesulfonyl chloride

: 95687-42-6
(2S,4R)-benzyl 4-(tosyloxy)-2-((tosyloxy)methyl)pyrrolidine-1-carboxylate

Guidance literature:: With pyridine; at 0 ℃;

Reference yield:

: 13504-85-3
(2S,4R)-1-(benzyloxycarbonyl)-4-hydroxypyrrolidine-2-carboxylic acid

: 95687-42-6
(2S,4R)-benzyl 4-(tosyloxy)-2-((tosyloxy)methyl)pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: BH₃*Me₂S / tetrahydrofuran / 0 °C

2: pyridine / 0 °C

With pyridine; dimethylsulfide borane complex; In tetrahydrofuran;