C₁₉H₁₇NO₂

Base Information

Chemical Name:C₁₉H₁₇NO₂
CAS No.:1338321-20-2
Molecular Formula:C₁₉H₁₇NO₂
Molecular Weight:291.349
Hs Code.:

C<sub>19</sub>H<sub>17</sub>NO<sub>2</sub>

Synonyms:C₁₉H₁₇NO₂

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Chemical Property of C₁₉H₁₇NO₂

Chemical Property:

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Technology Process of C₁₉H₁₇NO₂

There total 2 articles about C₁₉H₁₇NO₂ 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:

: 100-44-7
benzyl chloride

: 1338321-20-2
C₁₉H₁₇NO₂

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium tert-butylate; potassium iodide / N,N-dimethyl-formamide / 0.25 h / Inert atmosphere

1.2: 16 h / 20 °C / Inert atmosphere

2.1: dichloromethane / 16 h / 20 °C / Inert atmosphere

2.2: Inert atmosphere

With potassium tert-butylate; potassium iodide; In dichloromethane; N,N-dimethyl-formamide; 2.1: Wittig reaction;
DOI:10.1021/jm300197a

Reference yield:

: 1196-69-6
1H-indole-5-carboxaldehyde

: 1338321-20-2
C₁₉H₁₇NO₂

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium tert-butylate; potassium iodide / N,N-dimethyl-formamide / 0.25 h / Inert atmosphere

1.2: 16 h / 20 °C / Inert atmosphere

2.1: dichloromethane / 16 h / 20 °C / Inert atmosphere

2.2: Inert atmosphere

With potassium tert-butylate; potassium iodide; In dichloromethane; N,N-dimethyl-formamide; 2.1: Wittig reaction;
DOI:10.1021/jm300197a

Reference yield: 91.0%

: 1338321-20-2
C₁₉H₁₇NO₂

: 1338321-27-9
3-(1-benzyl-1H-indol-5-yl)acrylic acid

Guidance literature:: C₁₉H₁₇NO₂; With lithium hydroxide; In 1,4-dioxane; water; at 40 ℃; for 12h; Inert atmosphere;

With hydrogenchloride; In 1,4-dioxane; water; Inert atmosphere;
DOI:10.1021/jm300197a