(1S,4R)-6-exo-trimethylsilylmethyl-6-endo-hydroxy-2-benzyl-2-azabicyclo[2.2.1]heptan-3-one

Base Information

Chemical Name:(1S,4R)-6-exo-trimethylsilylmethyl-6-endo-hydroxy-2-benzyl-2-azabicyclo[2.2.1]heptan-3-one
CAS No.:640896-85-1
Molecular Formula:C₁₇H₂₅NO₂Si
Molecular Weight:303.476
Hs Code.:

Synonyms:(1S,4R)-6-exo-trimethylsilylmethyl-6-endo-hydroxy-2-benzyl-2-azabicyclo[2.2.1]heptan-3-one

Suppliers and Price of (1S,4R)-6-exo-trimethylsilylmethyl-6-endo-hydroxy-2-benzyl-2-azabicyclo[2.2.1]heptan-3-one

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 (1S,4R)-6-exo-trimethylsilylmethyl-6-endo-hydroxy-2-benzyl-2-azabicyclo[2.2.1]heptan-3-one

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (1S,4R)-6-exo-trimethylsilylmethyl-6-endo-hydroxy-2-benzyl-2-azabicyclo[2.2.1]heptan-3-one

There total 1 articles about (1S,4R)-6-exo-trimethylsilylmethyl-6-endo-hydroxy-2-benzyl-2-azabicyclo[2.2.1]heptan-3-one 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: 38.0%

: 13170-43-9
(trimethylsilyl)methylmagnesium chloride

: (1S,4R)-6-oxo-2-benzyl-2-azabicyclo[2.2.1]heptan-3-one

: 640896-85-1
(1S,4R)-6-exo-trimethylsilylmethyl-6-endo-hydroxy-2-benzyl-2-azabicyclo[2.2.1]heptan-3-one

Guidance literature:: In tetrahydrofuran; at -30 - 20 ℃;
DOI:10.1021/jm034162s

Reference yield: 86.0%

: 640896-85-1
(1S,4R)-6-exo-trimethylsilylmethyl-6-endo-hydroxy-2-benzyl-2-azabicyclo[2.2.1]heptan-3-one

: 640896-91-9
(1S,4R)-6-methylenyl-2-benzyl-2-azabicyclo[2.2.1]heptan-3-one

Guidance literature:: (1S,4R)-6-exo-trimethylsilylmethyl-6-endo-hydroxy-2-benzyl-2-azabicyclo[2.2.1]heptan-3-one; With dmap; trifluoroacetic anhydride; In tetrahydrofuran; at 20 ℃; for 3h;

With potassium fluoride; tetrabutylammomium bromide; In tetrahydrofuran; at 50 ℃; for 15h;
DOI:10.1021/jm034162s

Reference yield:

: 640896-85-1
(1S,4R)-6-exo-trimethylsilylmethyl-6-endo-hydroxy-2-benzyl-2-azabicyclo[2.2.1]heptan-3-one

: 640896-97-5,757942-73-7
(1S,3S)-3-amino-4-methylenyl-1-cyclopentanoic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: 4-dimethylaminopyridine; trifluoroacetic anhydride / tetrahydrofuran / 3 h / 20 °C

1.2: 86 percent / tetrabutylammonium bromide; potassium fluoride / tetrahydrofuran / 15 h / 50 °C

2.1: Na; liq. NH₃ / tetrahydrofuran; 2-methyl-propan-2-ol / 0.23 h / -78 - -30 °C

3.1: 0.065 g / aq. HCl; acetic acid / 5 h / 70 °C

With hydrogenchloride; dmap; ammonia; sodium; acetic acid; trifluoroacetic anhydride; In tetrahydrofuran; tert-butyl alcohol;
DOI:10.1021/jm034162s