(2S,3S,4R,5R,6R)-2-allyl-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)piperidine

Base Information

Chemical Name:(2S,3S,4R,5R,6R)-2-allyl-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)piperidine
CAS No.:1570183-94-6
Molecular Formula:C₃₇H₄₁NO₄
Molecular Weight:563.737
Hs Code.:

Synonyms:(2S,3S,4R,5R,6R)-2-allyl-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)piperidine

Suppliers and Price of (2S,3S,4R,5R,6R)-2-allyl-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)piperidine

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (2S,3S,4R,5R,6R)-2-allyl-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)piperidine

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2S,3S,4R,5R,6R)-2-allyl-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)piperidine

There total 2 articles about (2S,3S,4R,5R,6R)-2-allyl-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)piperidine 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:

: 24850-33-7
allyltributylstanane

: 1,N-didehydro-2,3,4,6-tetra-O-benzyl-deoxynojirimycin

: 1570183-94-6
(2S,3S,4R,5R,6R)-2-allyl-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)piperidine

: 950599-08-3
(2R,3S,4R,5R,6R)-2-allyl-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)piperidine

Guidance literature:: 1,N-didehydro-2,3,4,6-tetra-O-benzyl-deoxynojirimycin; With ytterbium(III) triflate; In tetrahydrofuran; at -25 ℃; for 0.166667h;

allyltributylstanane; In tetrahydrofuran; at -25 - 20 ℃;
DOI:10.1016/j.tet.2014.01.039

Reference yield:

: 77174-08-4
(3R,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)piperidin-2-one

: 1570183-94-6
(2S,3S,4R,5R,6R)-2-allyl-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)piperidine

: 950599-08-3
(2R,3S,4R,5R,6R)-2-allyl-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)piperidine

Guidance literature:: Multi-step reaction with 2 steps

1.1: Schwartz's reagent / tetrahydrofuran / 0.75 h / -25 - 20 °C / Inert atmosphere

2.1: ytterbium(III) triflate / tetrahydrofuran / 0.17 h / -25 °C

2.2: -25 - 20 °C

With Schwartz's reagent; ytterbium(III) triflate; In tetrahydrofuran;
DOI:10.1016/j.tet.2014.01.039

Reference yield:

: 1570183-94-6
(2S,3S,4R,5R,6R)-2-allyl-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)piperidine

: C₃₀H₃₄INO₄

Guidance literature:: (2S,3S,4R,5R,6R)-2-allyl-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)piperidine; With trimethylsilyl trifluoromethanesulfonate; In acetonitrile; at 0 ℃; for 0.0833333h; Inert atmosphere;

With N-iodo-succinimide; In acetonitrile; at 0 - 20 ℃; regioselective reaction; Inert atmosphere;
DOI:10.1021/acs.orglett.9b01712