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C13H15NO

Base Information Edit
C<sub>13</sub>H<sub>15</sub>NO

Synonyms:C13H15NO

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of C13H15NO Edit
Chemical Property:
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Technology Process of C13H15NO

There total 11 articles about C13H15NO 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:
Guidance literature:
Multi-step reaction with 7 steps
1.1: trifluoroacetic acid / dichloromethane / 18 h / 20 °C
2.1: diisobutylaluminium hydride / dichloromethane / 2 h / -78 °C
2.2: -78 - 20 °C
3.1: triethylamine / dmap / dichloromethane / 0 - 20 °C
4.1: boron trifluoride diethyl etherate / acetonitrile / 18 h / 20 °C / Inert atmosphere
5.1: ethyl acetate; cyclohexane / Resolution of diastereoisomeric mixture
6.1: potassium tert-butylate / tetrahydrofuran / 0.5 h / 20 °C
7.1: DAICEL AS-H / isopropyl alcohol; hexane; ethanol / Resolution of racemate
With boron trifluoride diethyl etherate; potassium tert-butylate; diisobutylaluminium hydride; triethylamine; trifluoroacetic acid; dmap; In tetrahydrofuran; ethanol; hexane; dichloromethane; cyclohexane; ethyl acetate; isopropyl alcohol; acetonitrile;
Guidance literature:
Multi-step reaction with 10 steps
1.1: copper(I) bromide; lithium bromide / tetrahydrofuran / 18 h / 0 °C / Inert atmosphere
2.1: water; lithium hydroxide monohydrate / tetrahydrofuran / 1 h / 50 °C
2.2: pH 1
3.1: potassium hydroxide; sodium tetrahydroborate / water / 10 - 20 °C
4.1: trifluoroacetic acid / dichloromethane / 18 h / 20 °C
5.1: diisobutylaluminium hydride / dichloromethane / 2 h / -78 °C
5.2: -78 - 20 °C
6.1: triethylamine / dmap / dichloromethane / 0 - 20 °C
7.1: boron trifluoride diethyl etherate / acetonitrile / 18 h / 20 °C / Inert atmosphere
8.1: ethyl acetate; cyclohexane / Resolution of diastereoisomeric mixture
9.1: potassium tert-butylate / tetrahydrofuran / 0.5 h / 20 °C
10.1: DAICEL AS-H / isopropyl alcohol; hexane; ethanol / Resolution of racemate
With sodium tetrahydroborate; lithium hydroxide monohydrate; boron trifluoride diethyl etherate; potassium tert-butylate; water; diisobutylaluminium hydride; triethylamine; trifluoroacetic acid; potassium hydroxide; copper(I) bromide; lithium bromide; dmap; In tetrahydrofuran; ethanol; hexane; dichloromethane; cyclohexane; water; ethyl acetate; isopropyl alcohol; acetonitrile;
Guidance literature:
Multi-step reaction with 6 steps
1.1: diisobutylaluminium hydride / dichloromethane / 2 h / -78 °C
1.2: -78 - 20 °C
2.1: triethylamine / dmap / dichloromethane / 0 - 20 °C
3.1: boron trifluoride diethyl etherate / acetonitrile / 18 h / 20 °C / Inert atmosphere
4.1: ethyl acetate; cyclohexane / Resolution of diastereoisomeric mixture
5.1: potassium tert-butylate / tetrahydrofuran / 0.5 h / 20 °C
6.1: DAICEL AS-H / isopropyl alcohol; hexane; ethanol / Resolution of racemate
With boron trifluoride diethyl etherate; potassium tert-butylate; diisobutylaluminium hydride; triethylamine; dmap; In tetrahydrofuran; ethanol; hexane; dichloromethane; cyclohexane; ethyl acetate; isopropyl alcohol; acetonitrile;
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