benzyl (3R)-3-[(tert-butoxycarbonyl)amino]-3-methylpiperidine-1-carboxylate

Base Information

Chemical Name:benzyl (3R)-3-[(tert-butoxycarbonyl)amino]-3-methylpiperidine-1-carboxylate
CAS No.:1169762-40-6
Molecular Formula:C₁₉H₂₈N₂O₄
Molecular Weight:348.442
Hs Code.:

Synonyms:benzyl (3R)-3-[(tert-butoxycarbonyl)amino]-3-methylpiperidine-1-carboxylate

Suppliers and Price of benzyl (3R)-3-[(tert-butoxycarbonyl)amino]-3-methylpiperidine-1-carboxylate

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 1 raw suppliers

Chemical Property of benzyl (3R)-3-[(tert-butoxycarbonyl)amino]-3-methylpiperidine-1-carboxylate

Chemical Property:

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of benzyl (3R)-3-[(tert-butoxycarbonyl)amino]-3-methylpiperidine-1-carboxylate

There total 5 articles about benzyl (3R)-3-[(tert-butoxycarbonyl)amino]-3-methylpiperidine-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:

: C₁₅H₁₈N₂O₃

: 75-65-0
tert-butyl alcohol

: 1169762-40-6
benzyl (3R)-3-[(tert-butoxycarbonyl)amino]-3-methylpiperidine-1-carboxylate

Guidance literature:: With potassium tert-butylate; at 80 ℃; for 2h;
DOI:10.1016/j.bmcl.2010.10.101

Reference yield:

: 1169762-38-2
C₁₅H₁₉NO₄

: 1169762-40-6
benzyl (3R)-3-[(tert-butoxycarbonyl)amino]-3-methylpiperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: diphenyl phosphoryl azide; triethylamine / toluene / 2 h / 100 °C / Inert atmosphere

2: potassium tert-butylate / toluene / 1 h / 40 °C / Inert atmosphere

With diphenyl phosphoryl azide; potassium tert-butylate; triethylamine; In toluene; 1: Curtius rearrangement;
DOI:10.1016/j.bmc.2011.07.042

Reference yield:

: 1169762-35-9
C₁₇H₂₃NO₄

: 1169762-40-6
benzyl (3R)-3-[(tert-butoxycarbonyl)amino]-3-methylpiperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydroxide / methanol; water / 24 h / Inert atmosphere; Reflux

1.2: Inert atmosphere; Acidic conditions

2.1: diphenyl phosphoryl azide; triethylamine / toluene / 2 h / 100 °C / Inert atmosphere

3.1: potassium tert-butylate / toluene / 1 h / 40 °C / Inert atmosphere

With diphenyl phosphoryl azide; potassium tert-butylate; triethylamine; sodium hydroxide; In methanol; water; toluene; 2.1: Curtius rearrangement;
DOI:10.1016/j.bmc.2011.07.042