(3R,4R,5R)-3,4,5-tris(benzyloxy)-6-benzyloxymethyl-2,3,4,5-tetrahydropyridine 1-oxide

Base Information

Chemical Name:(3R,4R,5R)-3,4,5-tris(benzyloxy)-6-benzyloxymethyl-2,3,4,5-tetrahydropyridine 1-oxide
CAS No.:1112338-13-2
Molecular Formula:C₃₄H₃₅NO₅
Molecular Weight:537.656
Hs Code.:

Synonyms:(3R,4R,5R)-3,4,5-tris(benzyloxy)-6-benzyloxymethyl-2,3,4,5-tetrahydropyridine 1-oxide

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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 (3R,4R,5R)-3,4,5-tris(benzyloxy)-6-benzyloxymethyl-2,3,4,5-tetrahydropyridine 1-oxide

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Technology Process of (3R,4R,5R)-3,4,5-tris(benzyloxy)-6-benzyloxymethyl-2,3,4,5-tetrahydropyridine 1-oxide

There total 2 articles about (3R,4R,5R)-3,4,5-tris(benzyloxy)-6-benzyloxymethyl-2,3,4,5-tetrahydropyridine 1-oxide 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: 55.0%

: 1,3,4,5-tetra-O-benzyl-6-O-methanesulfonyl-D-fructose O-(tertbutyldiphenylsilyl)oxime

: 1112338-13-2
(3R,4R,5R)-3,4,5-tris(benzyloxy)-6-benzyloxymethyl-2,3,4,5-tetrahydropyridine 1-oxide

: 1112338-46-1
3,4,5-tri-O-benzyl-6-O-methanesulfonyl-D-fructose oxime

Guidance literature:: With TBAF on SiO₂; In tetrahydrofuran; at 0 - 20 ℃;
DOI:10.1021/jo802255t

Reference yield: 40.0%

: 1,3,4,5-tetra-O-benzyl-6-O-methanesulfonyl-D-fructose O-(tertbutyldiphenylsilyl)oxime

: 1112338-13-2
(3R,4R,5R)-3,4,5-tris(benzyloxy)-6-benzyloxymethyl-2,3,4,5-tetrahydropyridine 1-oxide

: (4R,5S,6R)-4,5,6-tris(benzyloxy)-3-[(benzyloxy)methyl]-4,5,6,7-tetrahydro-1,2-oxazepine

Guidance literature:: With tetrabutylammonium triphenyldifluorosilicate; In tetrahydrofuran; at 65 ℃; for 24h; Overall yield = 70 %; Molecular sieve;
DOI:10.1002/ejoc.201600478