((2S,3S,4R,5R,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-1-butyl-piperidin-2-yl)-methanol

Base Information

Chemical Name:((2S,3S,4R,5R,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-1-butyl-piperidin-2-yl)-methanol
CAS No.:182124-74-9
Molecular Formula:C₃₉H₄₇NO₅
Molecular Weight:609.806
Hs Code.:

Synonyms:((2S,3S,4R,5R,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-1-butyl-piperidin-2-yl)-methanol

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Chemical Property of ((2S,3S,4R,5R,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-1-butyl-piperidin-2-yl)-methanol

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Technology Process of ((2S,3S,4R,5R,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-1-butyl-piperidin-2-yl)-methanol

There total 5 articles about ((2S,3S,4R,5R,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-1-butyl-piperidin-2-yl)-methanol 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: 75.0%

: 1055040-06-6
(2R,3R,4S,5S,6S)-3,4,5-Tris-benzyloxy-2-benzyloxymethyl-1-butyl-6-methoxymethoxymethyl-piperidine

: 182124-74-9
((2S,3S,4R,5R,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-1-butyl-piperidin-2-yl)-methanol

Guidance literature:: With hydrogenchloride; In tetrahydrofuran; water; at 50 ℃;
DOI:10.1021/jo960362i

Reference yield:

: 162333-06-4
3,4,5,7-tetra-O-benzyl-1-O-(methoxymethyl)-D-xylo-2,6-heptodiulose

: 182124-74-9
((2S,3S,4R,5R,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-1-butyl-piperidin-2-yl)-methanol

Guidance literature:: Multi-step reaction with 4 steps

1: ammonium formate, NaBH₃CN / methanol / 0.5 h / Ambient temperature

2: 1.) MeMgI / 1.) THF, room temperature, 5 min, 2) room temperature, 2 h

3: 82 percent / BH₃ / tetrahydrofuran / 1.5 h / Heating

4: 75 percent / aq. HCl / tetrahydrofuran; H₂O / 50 °C

With hydrogenchloride; methyl magnesium iodide; borane; ammonium formate; sodium cyanoborohydride; In tetrahydrofuran; methanol; water;
DOI:10.1021/jo960362i

Reference yield:

: 162333-05-3
3,4,5,7-tetra-O-benzyl-2,6-dideoxy-2,6-imino-1-O-(methoxymethyl)-D-glycero-D-gulo-heptitol

: 182124-74-9
((2S,3S,4R,5R,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-1-butyl-piperidin-2-yl)-methanol

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) MeMgI / 1.) THF, room temperature, 5 min, 2) room temperature, 2 h

2: 82 percent / BH₃ / tetrahydrofuran / 1.5 h / Heating

3: 75 percent / aq. HCl / tetrahydrofuran; H₂O / 50 °C

With hydrogenchloride; methyl magnesium iodide; borane; In tetrahydrofuran; water;
DOI:10.1021/jo960362i