N-benzyl-2-ethylhexanamide

Base Information

Chemical Name:N-benzyl-2-ethylhexanamide
CAS No.:349120-32-7
Molecular Formula:C₁₅H₂₃NO
Molecular Weight:233.354
Hs Code.:

Synonyms:

Suppliers and Price of N-benzyl-2-ethylhexanamide

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 N-benzyl-2-ethylhexanamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-benzyl-2-ethylhexanamide

There total 6 articles about N-benzyl-2-ethylhexanamide 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: 90.0%

: 879881-82-0
(S)-2-Ethyl-3-(toluene-4-sulfonyl)-hexanoic acid benzylamide

: 879881-86-4,349120-32-7
(R)-2-Ethyl-hexanoic acid benzylamide

Guidance literature:: With sodium amalgam; In methanol; at 0 ℃; for 2h;
DOI:10.1080/00397910500374740

Reference yield:

: 879881-79-5
(R)-5-Chloro-5-(toluene-4-sulfonyl)-octan-4-one

: 879881-86-4,349120-32-7
(R)-2-Ethyl-hexanoic acid benzylamide

Guidance literature:: Multi-step reaction with 2 steps

1: 97 percent / NaH / tetrahydrofuran / 2.5 h / 0 °C

2: 90 percent / Na amalgam / methanol / 2 h / 0 °C

With sodium amalgam; sodium hydride; In tetrahydrofuran; methanol; 1: Favorskii asymmetric rearrangement;
DOI:10.1080/00397910500374740

Reference yield:

: 879881-77-3
(R)-5-Chloro-5-(toluene-4-sulfonyl)-octan-4-ol

: 879881-86-4,349120-32-7
(R)-2-Ethyl-hexanoic acid benzylamide

Guidance literature:: Multi-step reaction with 3 steps

1: 97 percent / NaH / tetrahydrofuran / 2.5 h / 0 °C

2: 90 percent / Na amalgam / methanol / 2 h / 0 °C

With sodium amalgam; sodium hydride; In tetrahydrofuran; methanol; 1: Swern oxidation / 2: Favorskii asymmetric rearrangement;
DOI:10.1080/00397910500374740