C₁₈H₁₆FNO₃S

Base Information Edit

Chemical Name:C₁₈H₁₆FNO₃S
CAS No.:1374233-05-2
Molecular Formula:C₁₈H₁₆FNO₃S
Molecular Weight:345.394
Hs Code.:
Mol file:1374233-05-2.mol

C<sub>18</sub>H<sub>16</sub>FNO<sub>3</sub>S

Synonyms:C₁₈H₁₆FNO₃S

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Chemical Property of C₁₈H₁₆FNO₃S Edit

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Technology Process of C₁₈H₁₆FNO₃S

There total 8 articles about C₁₈H₁₆FNO₃S 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:

: 1374233-04-1
C₂₄H₃₀FNO₄SSi

: 1374233-05-2
C₁₈H₁₆FNO₃S

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 0.5h;

Reference yield:

: 4964-76-5
7-methoxyquinoline

: 1374233-05-2
C₁₈H₁₆FNO₃S

Guidance literature:: Multi-step reaction with 7 steps

1.1: hydrogen / platinum(IV) oxide / methanol / 16 h / 20 °C

2.1: triethylamine / dichloromethane / 0.5 h / 0 - 20 °C

3.1: N-iodo-succinimide / chloroform / 16 h / 0 - 20 °C

4.1: boron tribromide / dichloromethane / 1 h / -20 °C

4.2: Cooling with ice

5.1: triethylamine / dmap / tetrahydrofuran / 3 h / 0 - 20 °C

6.1: piperidine / bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; tri-tert-butyl phosphine / N,N-dimethyl-formamide / 80 °C / Inert atmosphere

7.1: hydrogenchloride / 1,4-dioxane / 0.5 h / 20 °C

With piperidine; hydrogenchloride; N-iodo-succinimide; hydrogen; boron tribromide; triethylamine; dmap; platinum(IV) oxide; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; tri-tert-butyl phosphine; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; chloroform; N,N-dimethyl-formamide;

Reference yield:

: 19500-61-9
7-methoxy-1,2,3,4-tetrahydroquinoline

: 1374233-05-2
C₁₈H₁₆FNO₃S

Guidance literature:: Multi-step reaction with 6 steps

1.1: triethylamine / dichloromethane / 0.5 h / 0 - 20 °C

2.1: N-iodo-succinimide / chloroform / 16 h / 0 - 20 °C

3.1: boron tribromide / dichloromethane / 1 h / -20 °C

3.2: Cooling with ice

4.1: triethylamine / dmap / tetrahydrofuran / 3 h / 0 - 20 °C

5.1: piperidine / bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; tri-tert-butyl phosphine / N,N-dimethyl-formamide / 80 °C / Inert atmosphere

6.1: hydrogenchloride / 1,4-dioxane / 0.5 h / 20 °C

With piperidine; hydrogenchloride; N-iodo-succinimide; boron tribromide; triethylamine; dmap; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; tri-tert-butyl phosphine; In tetrahydrofuran; 1,4-dioxane; dichloromethane; chloroform; N,N-dimethyl-formamide;