(R)-3-Oxo-6-(3-oxo-cyclohex-1-enylamino)-undecanoic acid tert-butyl ester

Base Information

Chemical Name:(R)-3-Oxo-6-(3-oxo-cyclohex-1-enylamino)-undecanoic acid tert-butyl ester
CAS No.:120791-01-7
Molecular Formula:C₂₁H₃₅NO₄
Molecular Weight:365.513
Hs Code.:

Synonyms:(R)-3-Oxo-6-(3-oxo-cyclohex-1-enylamino)-undecanoic acid tert-butyl ester

Suppliers and Price of (R)-3-Oxo-6-(3-oxo-cyclohex-1-enylamino)-undecanoic acid tert-butyl ester

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 (R)-3-Oxo-6-(3-oxo-cyclohex-1-enylamino)-undecanoic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (R)-3-Oxo-6-(3-oxo-cyclohex-1-enylamino)-undecanoic acid tert-butyl ester

There total 3 articles about (R)-3-Oxo-6-(3-oxo-cyclohex-1-enylamino)-undecanoic acid tert-butyl ester 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:

: 72479-05-1
(S)-(-)-5-(Bromomethyl)-2-pyrrolidinone

: 120791-01-7
(R)-3-Oxo-6-(3-oxo-cyclohex-1-enylamino)-undecanoic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 79 percent / CuCN / diethyl ether; hexane; tetrahydrofuran / 1.) -40 deg C, 2 h, 2.) -15 deg C, 14 h

3: 1.) LDA / 1.) THF, hexane, -78 deg C, 45 min, 2.) THF, hexane, -78 deg C, 1.25 h; -40 deg C, 1.5 h; 0 deg C, 1 h

With lithium diisopropyl amide; In tetrahydrofuran; diethyl ether; hexane;
DOI:10.1021/ja00195a042

Reference yield:

: 118015-99-9
(R)-5-Pentyl-2-pyrrolidinone

: 120791-01-7
(R)-3-Oxo-6-(3-oxo-cyclohex-1-enylamino)-undecanoic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

2: 1.) LDA / 1.) THF, hexane, -78 deg C, 45 min, 2.) THF, hexane, -78 deg C, 1.25 h; -40 deg C, 1.5 h; 0 deg C, 1 h

With lithium diisopropyl amide;
DOI:10.1021/ja00195a042

Reference yield:

: 540-88-5
acetic acid tert-butyl ester

: 120791-00-6
(R)-4-(3-Oxo-cyclohex-1-enylamino)-nonanoic acid methyl ester

: 120791-01-7
(R)-3-Oxo-6-(3-oxo-cyclohex-1-enylamino)-undecanoic acid tert-butyl ester

Guidance literature:: With lithium diisopropyl amide; Yield given. Multistep reaction; 1.) THF, hexane, -78 deg C, 45 min, 2.) THF, hexane, -78 deg C, 1.25 h; -40 deg C, 1.5 h; 0 deg C, 1 h;
DOI:10.1021/ja00195a042