tert-Butyl(butylidene)amine

Base Information

• Chemical Name: tert-Butyl(butylidene)amine
• CAS No.: 6852-59-1
• Molecular Formula: C₈H₁₇N
• Molecular Weight: 127.23
• DSSTox Substance ID: DTXSID801294105
• Nikkaji Number: J1.207.887K,J1.901.335I

Synonyms:tert-Butyl(butylidene)amine;6852-59-1;N-t-butylbutaneimine;N-butylidene-t-butylamine;SCHEMBL7111853;SCHEMBL22952855;IQQAQKRUBBGOPB-UHFFFAOYSA-N;DTXSID801294105;N-Butylidene-2-methyl-2-propanamine;EN300-209497

Chemical Property of tert-Butyl(butylidene)amine

Chemical Property:

• XLogP3: 1.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 127.136099547
• Heavy Atom Count: 9
• Complexity: 87.2

Purity/Quality:

97% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CCCC=NC(C)(C)C

Technology Process of tert-Butyl(butylidene)amine

There total 1 articles about tert-Butyl(butylidene)amine 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: 33.0%

1-tert-butyl-4-methyl-1-aza-1,3-butadiene (6943-47-1) → tert-butyl-butyliden-amine (6852-59-1) + n-butyl-tert-butylamine (16486-74-1)

Guidance literature:

With 1,4-diaza-bicyclo[2.2.2]octane; 2,4,6-trimethylphenylbis(pentafluorophenyl)borane; hydrogen; In benzene-d6; at 20 ℃; for 42h; under 3040.2 Torr; Inert atmosphere;

DOI:10.1002/chem.201102438

Reference yield: 73.0%

tert-butyl-butyliden-amine (6852-59-1) + (1R,2S,3R,6S)-3-Hydroxy-9-aza-bicyclo[4.2.1]nonane-2,9-dicarboxylic acid 9-benzyl ester 2-methyl ester (382141-47-1) → (1R,2S,3R,6S)-2-{2-[(E)-tert-Butylimino-methyl]-butyryl}-3-hydroxy-9-aza-bicyclo[4.2.1]nonane-9-carboxylic acid benzyl ester (382141-48-2)

Guidance literature:

With lithium diisopropyl amide; In tetrahydrofuran; at 0 ℃;

DOI:10.1016/S0040-4039(01)01583-0

Reference yield: 61.0%

tert-butyl-butyliden-amine (6852-59-1) + [((2,6-diisopropylphenyl)BDI)CaH*(THF)]2 → C41H65CaN3O

Guidance literature:

at 60 ℃; for 1h; Inert atmosphere; Schlenk technique;

DOI:10.1021/acs.organomet.0c00226

upstream raw materials:

1-tert-butyl-4-methyl-1-aza-1,3-butadiene

Downstream raw materials:

tert-butyl-(1-propyl-prop-2-ynyl)-amine

1-tert-butyl-3,5-diethyl-2-phenyl-1,2-dihydro-1,2-λ³-azaphosphinine

1-tert-butyl-3-propyl-4-ethyl-2-phenyl-2-oxo-1,2,4-azaphospholene

(1R,2S,3R,6S)-2-{2-[(E)-tert-Butylimino-methyl]-butyryl}-3-hydroxy-9-aza-bicyclo[4.2.1]nonane-9-carboxylic acid benzyl ester

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