(1S,4R)-1-<(2S)-2<(2R)-2-Hydroxy-2-phenyl-1-ethyl>-1-piperidylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-on

Base Information

• Chemical Name: (1S,4R)-1-<(2S)-2<(2R)-2-Hydroxy-2-phenyl-1-ethyl>-1-piperidylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-on
• CAS No.: 112653-24-4
• Molecular Formula: C₂₃H₃₁NO₄
• Molecular Weight: 385.503
• Mol file: 112653-24-4.mol

Synonyms:(1S,4R)-1-<(2S)-2<(2R)-2-Hydroxy-2-phenyl-1-ethyl>-1-piperidylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-on

Chemical Property of (1S,4R)-1-<(2S)-2<(2R)-2-Hydroxy-2-phenyl-1-ethyl>-1-piperidylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-on

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (1S,4R)-1-<(2S)-2<(2R)-2-Hydroxy-2-phenyl-1-ethyl>-1-piperidylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-on

There total 3 articles about (1S,4R)-1-<(2S)-2<(2R)-2-Hydroxy-2-phenyl-1-ethyl>-1-piperidylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-on 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: 44.8%

(1S,4R)-1-<(2S)-2-(2-oxo-2-phenyl-1-ethyl-)-1-piperidylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-on (111504-84-8) → (1S,4R)-1-<(2S)-2<(2S)-2-Hydroxy-2-phenyl-1-ethyl>-1-piperidylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-on (112653-25-5) + (1S,4R)-1-<(2S)-2<(2R)-2-Hydroxy-2-phenyl-1-ethyl>-1-piperidylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-on (112653-24-4)

Guidance literature:

With sodium tetrahydroborate; In ethanol; for 15h; Ambient temperature;

Reference yield:

1-styrenyloxytrimethylsilane (13735-81-4) → (1S,4R)-1-<(2S)-2<(2R)-2-Hydroxy-2-phenyl-1-ethyl>-1-piperidylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-on (112653-24-4)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) TiCl₄, HCl / 1.) -78 deg C, 0.5 h, CH₂Cl₂, 2.) 45 min, CH₂Cl₂

2: 44.8 percent / NaBH₄ / ethanol / 15 h / Ambient temperature

With hydrogenchloride; sodium tetrahydroborate; titanium tetrachloride; In ethanol;

Reference yield:

(1S,4R)-1-(1,2,3,4-Tetrahydro-1-pyridyl-carbonyl)-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-on (111504-83-7) → (1S,4R)-1-<(2S)-2<(2R)-2-Hydroxy-2-phenyl-1-ethyl>-1-piperidylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-on (112653-24-4)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) TiCl₄, HCl / 1.) -78 deg C, 0.5 h, CH₂Cl₂, 2.) 45 min, CH₂Cl₂

2: 44.8 percent / NaBH₄ / ethanol / 15 h / Ambient temperature

With hydrogenchloride; sodium tetrahydroborate; titanium tetrachloride; In ethanol;

upstream raw materials:

(1S,4R)-1-<(2S)-2-(2-oxo-2-phenyl-1-ethyl-)-1-piperidylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-on

1-styrenyloxytrimethylsilane

(1S,4R)-1-(1,2,3,4-Tetrahydro-1-pyridyl-carbonyl)-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-on

Downstream raw materials:

1-phenyl-2-[(2S)-piperidin-2-yl]-(1R)-ethan-1-ol