C₁₇H₁₈FNO₂

Base Information

Chemical Name:C₁₇H₁₈FNO₂
CAS No.:1416889-55-8
Molecular Formula:C₁₇H₁₈FNO₂
Molecular Weight:287.334
Hs Code.:

C<sub>17</sub>H<sub>18</sub>FNO<sub>2</sub>

Synonyms:

Suppliers and Price of C₁₇H₁₈FNO₂

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 C₁₇H₁₈FNO₂

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₁₇H₁₈FNO₂

There total 5 articles about C₁₇H₁₈FNO₂ 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:

: 1416889-54-7
(2S,3R)-methyl 3-(4-fluorophenyl)-4-nitro-2-phenylbutanoate

: 1416889-55-8
C₁₇H₁₈FNO₂

Guidance literature:: With hydrogen; In methanol; at 20 ℃; for 12h;
DOI:10.1039/c2ob26950c

Reference yield:

: 1416889-53-6
(2S,3R)-3-(4-fluorophenyl)-4-nitro-2-phenylbutanoic acid

: 1416889-55-8
C₁₇H₁₈FNO₂

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / 12 h / 0 - 20 °C

2: hydrogen / methanol / 12 h / 20 °C

With thionyl chloride; hydrogen; In methanol;
DOI:10.1039/c2ob26950c

Reference yield:

: 17123-83-0
N-(phenylacetyl)morpholine

: 1416889-55-8
C₁₇H₁₈FNO₂

Guidance literature:: Multi-step reaction with 5 steps

1.1: lithium / tetrahydrofuran

1.2: 2 h / -78 °C / Inert atmosphere

2.1: (S,E)-N-benzhydryl-1-(N,N'-dicyclohexylcarbamimidoyl)pyrrolidine-2-carboxamide / toluene / 12 h / 0 °C / Inert atmosphere; Molecular sieve

2.2: 8 h / 0 °C / Inert atmosphere; Molecular sieve

3.1: tetrabutyl ammonium fluoride; dihydrogen peroxide / tetrahydrofuran / 2 h / 20 °C

4.1: thionyl chloride / 12 h / 0 - 20 °C

5.1: hydrogen / methanol / 12 h / 20 °C

With thionyl chloride; (S,E)-N-benzhydryl-1-(N,N'-dicyclohexylcarbamimidoyl)pyrrolidine-2-carboxamide; tetrabutyl ammonium fluoride; hydrogen; dihydrogen peroxide; lithium; In tetrahydrofuran; methanol; toluene; 2.1: |Michael Addition / 2.2: |Michael Addition;
DOI:10.1039/c2ob26950c