tert-butyl (3S,αR)-3-(N-benzyl-N-α-methylbenzylamino)-3-(piperon-3-yl)propanoate

Base Information

Chemical Name:tert-butyl (3S,αR)-3-(N-benzyl-N-α-methylbenzylamino)-3-(piperon-3-yl)propanoate
CAS No.:911224-80-1
Molecular Formula:C₂₉H₃₃NO₄
Molecular Weight:459.585
Hs Code.:

Synonyms:tert-butyl (3S,αR)-3-(N-benzyl-N-α-methylbenzylamino)-3-(piperon-3-yl)propanoate

Suppliers and Price of tert-butyl (3S,αR)-3-(N-benzyl-N-α-methylbenzylamino)-3-(piperon-3-yl)propanoate

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 tert-butyl (3S,αR)-3-(N-benzyl-N-α-methylbenzylamino)-3-(piperon-3-yl)propanoate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of tert-butyl (3S,αR)-3-(N-benzyl-N-α-methylbenzylamino)-3-(piperon-3-yl)propanoate

There total 3 articles about tert-butyl (3S,αR)-3-(N-benzyl-N-α-methylbenzylamino)-3-(piperon-3-yl)propanoate 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: 91.0%

: 181517-76-0
3-(3',4'-methylenedioxyphenyl)-(E)-propenoic acid tert-butyl ester

: 38235-77-7
(R)-N-benzyl-1-phenylethylamine

: 911224-80-1
tert-butyl (3S,αR)-3-(N-benzyl-N-α-methylbenzylamino)-3-(piperon-3-yl)propanoate

Guidance literature:: (R)-N-benzyl-1-phenylethylamine; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 0.5h;

3-(3',4'-methylenedioxyphenyl)-(E)-propenoic acid tert-butyl ester; In tetrahydrofuran; hexane; at -78 ℃; for 3h; Further stages.;
DOI:10.1016/j.tetasy.2007.06.008

Reference yield:

: 120-57-0,30024-74-9
piperonal

: 911224-80-1
tert-butyl (3S,αR)-3-(N-benzyl-N-α-methylbenzylamino)-3-(piperon-3-yl)propanoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-BuLi / tetrahydrofuran; hexane / 0.5 h / -78 °C

1.2: 93 percent / tetrahydrofuran; hexane / -78 - 20 °C

2.1: n-BuLi / tetrahydrofuran; hexane / 0.5 h / -78 °C

2.2: 91 percent / tetrahydrofuran; hexane / 3 h / -78 °C

With n-butyllithium; In tetrahydrofuran; hexane; 1.1: Horner-Wadsworth-Emmons reaction;
DOI:10.1016/j.tetasy.2007.06.008

Reference yield:

: 27784-76-5
tert-butyl diethylphosphonoacetate

: 911224-80-1
tert-butyl (3S,αR)-3-(N-benzyl-N-α-methylbenzylamino)-3-(piperon-3-yl)propanoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-BuLi / tetrahydrofuran; hexane / 0.5 h / -78 °C

1.2: 93 percent / tetrahydrofuran; hexane / -78 - 20 °C

2.1: n-BuLi / tetrahydrofuran; hexane / 0.5 h / -78 °C

2.2: 91 percent / tetrahydrofuran; hexane / 3 h / -78 °C

With n-butyllithium; In tetrahydrofuran; hexane; 1.1: Horner-Wadsworth-Emmons reaction;
DOI:10.1016/j.tetasy.2007.06.008