(2S,3R,6R)-3-benzyloxy-6-dodecyl-1-(methoxycarbonyl)-2-(methoxymethoxy)methylpiperidine

Base Information

Chemical Name:(2S,3R,6R)-3-benzyloxy-6-dodecyl-1-(methoxycarbonyl)-2-(methoxymethoxy)methylpiperidine
CAS No.:153198-50-6
Molecular Formula:C₂₉H₄₉NO₅
Molecular Weight:491.712
Hs Code.:

Synonyms:(2S,3R,6R)-3-benzyloxy-6-dodecyl-1-(methoxycarbonyl)-2-(methoxymethoxy)methylpiperidine

Suppliers and Price of (2S,3R,6R)-3-benzyloxy-6-dodecyl-1-(methoxycarbonyl)-2-(methoxymethoxy)methylpiperidine

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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,3R,6R)-3-benzyloxy-6-dodecyl-1-(methoxycarbonyl)-2-(methoxymethoxy)methylpiperidine

Chemical Property:

Purity/Quality:

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Technology Process of (2S,3R,6R)-3-benzyloxy-6-dodecyl-1-(methoxycarbonyl)-2-(methoxymethoxy)methylpiperidine

There total 9 articles about (2S,3R,6R)-3-benzyloxy-6-dodecyl-1-(methoxycarbonyl)-2-(methoxymethoxy)methylpiperidine 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: 79.0%

: 157331-03-8
(2S,3R,6S)-3-benzyloxy-6-<(Z)-1-dodecenyl>-1-(methoxycarbonyl)-2-(methoxymethoxy)methylpiperidine

: 153198-50-6
(2S,3R,6R)-3-benzyloxy-6-dodecyl-1-(methoxycarbonyl)-2-(methoxymethoxy)methylpiperidine

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; for 2h;
DOI:10.1016/S0040-4020(01)85638-6

Reference yield:

: 693-67-4
bromoundecane

: 153198-50-6
(2S,3R,6R)-3-benzyloxy-6-dodecyl-1-(methoxycarbonyl)-2-(methoxymethoxy)methylpiperidine

Guidance literature:: Multi-step reaction with 4 steps

1: 92 percent / 12 h / 100 °C

2: sodium amide / tetrahydrofuran / 2 h / Heating

3: 59 percent / tetrahydrofuran / 0.17 h / 0 °C

4: 79 percent / hydrogen / 10percent palladium on charcoal / ethanol / 2 h

With hydrogen; sodium amide; palladium on activated charcoal; In tetrahydrofuran; ethanol;
DOI:10.1016/S0040-4020(01)85638-6

Reference yield:

: 60669-22-9
n-undecyltriphenylphosphonium bromide

: 153198-50-6
(2S,3R,6R)-3-benzyloxy-6-dodecyl-1-(methoxycarbonyl)-2-(methoxymethoxy)methylpiperidine

Guidance literature:: Multi-step reaction with 3 steps

1: sodium amide / tetrahydrofuran / 2 h / Heating

2: 59 percent / tetrahydrofuran / 0.17 h / 0 °C

3: 79 percent / hydrogen / 10percent palladium on charcoal / ethanol / 2 h

With hydrogen; sodium amide; palladium on activated charcoal; In tetrahydrofuran; ethanol;
DOI:10.1016/S0040-4020(01)85638-6