(-)-(Z)-2-benzylamino-2-(3-trimethylysilylprop-2-ynyl)cyclohexanone

Base Information

• Chemical Name: (-)-(Z)-2-benzylamino-2-(3-trimethylysilylprop-2-ynyl)cyclohexanone
• CAS No.: 164221-00-5
• Molecular Formula: C₁₉H₂₉NOSi
• Molecular Weight: 315.531
• Mol file: 164221-00-5.mol

Synonyms:(-)-(Z)-2-benzylamino-2-(3-trimethylysilylprop-2-ynyl)cyclohexanone

Chemical Property of (-)-(Z)-2-benzylamino-2-(3-trimethylysilylprop-2-ynyl)cyclohexanone

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (-)-(Z)-2-benzylamino-2-(3-trimethylysilylprop-2-ynyl)cyclohexanone

There total 5 articles about (-)-(Z)-2-benzylamino-2-(3-trimethylysilylprop-2-ynyl)cyclohexanone 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: 67.0%

(-)-2-benzylamino-2-(3-trimethylysilylprop-2-ynyl)cyclohexanone (164220-99-9) → (-)-(Z)-2-benzylamino-2-(3-trimethylysilylprop-2-ynyl)cyclohexanone (164221-00-5)

Guidance literature:

With quinoline; hydrogen; Pd-BaSO₄; In ethanol; Ambient temperature;

DOI:10.1016/0040-4039(95)00681-2

Reference yield:

2-[(trimethylsilyl)oxy]cyclohex-2-en-1-one (51128-50-8) → (-)-(Z)-2-benzylamino-2-(3-trimethylysilylprop-2-ynyl)cyclohexanone (164221-00-5)

Guidance literature:

Multi-step reaction with 6 steps

1: 48 percent / TMEDA / diethyl ether / -78 - -40 °C

2: 41 percent / DMAP / CH₂Cl₂ / 20 h / Ambient temperature

3: 81 percent / nBu₄NOH, H₂O / CH₂Cl₂; ethanol; propan-2-ol / 0.25 h

4: toluene / 3 h / Heating

5: bis-(2-methoxy-ethyl) ether / Heating

6: 67 percent / H₂, quinoline / Pd/BaSO₄

With quinoline; dmap; N,N,N,N,-tetramethylethylenediamine; tetra(n-butyl)ammonium hydroxide; water; hydrogen; Pd-BaSO₄; In diethyl ether; ethanol; dichloromethane; diethylene glycol dimethyl ether; isopropyl alcohol; toluene;

DOI:10.1016/0040-4020(96)00317-1

Reference yield:

2-hydroxy-2-(3-trimethylsilylprop-2-ynyl)cyclohexanone (128939-10-6) → (-)-(Z)-2-benzylamino-2-(3-trimethylysilylprop-2-ynyl)cyclohexanone (164221-00-5)

Guidance literature:

Multi-step reaction with 5 steps

1: 41 percent / DMAP / CH₂Cl₂ / 20 h / Ambient temperature

2: 81 percent / nBu₄NOH, H₂O / CH₂Cl₂; ethanol; propan-2-ol / 0.25 h

3: toluene / 3 h / Heating

4: bis-(2-methoxy-ethyl) ether / Heating

5: 67 percent / H₂, quinoline / Pd/BaSO₄

With quinoline; dmap; tetra(n-butyl)ammonium hydroxide; water; hydrogen; Pd-BaSO₄; In ethanol; dichloromethane; diethylene glycol dimethyl ether; isopropyl alcohol; toluene;

DOI:10.1016/0040-4020(96)00317-1

upstream raw materials:

(-)-2-benzylamino-2-(3-trimethylysilylprop-2-ynyl)cyclohexanone

2-[(trimethylsilyl)oxy]cyclohex-2-en-1-one

2-hydroxy-2-(3-trimethylsilylprop-2-ynyl)cyclohexanone

(R)-2-[(Z)-Benzylimino]-1-(3-trimethylsilanyl-prop-2-ynyl)-cyclohexanol