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C14H21IO

Base Information
  • Chemical Name:C14H21IO
  • CAS No.:1620643-52-8
  • Molecular Formula:C14H21IO
  • Molecular Weight:332.225
  • Hs Code.:
C<sub>14</sub>H<sub>21</sub>IO

Synonyms:C14H21IO

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Chemical Property of C14H21IO
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Technology Process of C14H21IO

There total 1 articles about C14H21IO 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:
With 1H-imidazole; iodine; triphenylphosphine; In diethyl ether; acetonitrile; at 0 - 20 ℃; for 13h; Inert atmosphere;
DOI:10.1002/anie.201400305
Guidance literature:
Multi-step reaction with 9 steps
1.1: dimethyl sulfoxide / 39 h / 20 °C / Inert atmosphere
2.1: sodium iodide; chloro-trimethyl-silane / acetonitrile / 2 h / 20 °C / Inert atmosphere
3.1: triphenylphosphine; 1H-imidazole; iodine / diethyl ether; acetonitrile / 12 h / 0 - 20 °C / Inert atmosphere
4.1: diisobutylaluminium hydride / dichloromethane; hexane / 3 h / -78 °C / Inert atmosphere
5.1: propionic acid; pyrrolidine / water; isopropyl alcohol / 18 h / 55 °C / Inert atmosphere
6.1: cerium(III) chloride heptahydrate / ethanol / 0.5 h / 0 °C / Inert atmosphere
6.2: 2 h / 0 °C / Inert atmosphere
7.1: 1H-imidazole / tetrahydrofuran / 2 h / 0 - 20 °C / Inert atmosphere
8.1: tert.-butyl lithium / diethyl ether; pentane / 0.08 h / -78 °C / Inert atmosphere
8.2: 4 h / 20 °C / Inert atmosphere
9.1: Schwartz's reagent / benzene / 24 h / 20 °C / Inert atmosphere
9.2: 1 h
9.3: 20 h / 20 °C / Darkness
With pyrrolidine; 1H-imidazole; Schwartz's reagent; chloro-trimethyl-silane; cerium(III) chloride heptahydrate; iodine; tert.-butyl lithium; diisobutylaluminium hydride; propionic acid; triphenylphosphine; sodium iodide; In tetrahydrofuran; diethyl ether; ethanol; hexane; dichloromethane; water; dimethyl sulfoxide; isopropyl alcohol; acetonitrile; pentane; benzene; 9.3: |Suzuki-Miyaura Coupling;
DOI:10.1002/anie.201400305
Guidance literature:
Multi-step reaction with 10 steps
1.1: dimethyl sulfoxide / 39 h / 20 °C / Inert atmosphere
2.1: sodium iodide; chloro-trimethyl-silane / acetonitrile / 2 h / 20 °C / Inert atmosphere
3.1: triphenylphosphine; 1H-imidazole; iodine / diethyl ether; acetonitrile / 12 h / 0 - 20 °C / Inert atmosphere
4.1: diisobutylaluminium hydride / dichloromethane; hexane / 3 h / -78 °C / Inert atmosphere
5.1: propionic acid; pyrrolidine / water; isopropyl alcohol / 18 h / 55 °C / Inert atmosphere
6.1: cerium(III) chloride heptahydrate / ethanol / 0.5 h / 0 °C / Inert atmosphere
6.2: 2 h / 0 °C / Inert atmosphere
7.1: 1H-imidazole / tetrahydrofuran / 2 h / 0 - 20 °C / Inert atmosphere
8.1: tert.-butyl lithium / diethyl ether; pentane / 0.08 h / -78 °C / Inert atmosphere
8.2: 4 h / 20 °C / Inert atmosphere
9.1: Schwartz's reagent / benzene / 24 h / 20 °C / Inert atmosphere
9.2: 1 h
9.3: 20 h / 20 °C / Darkness
10.1: sodium hydride / tetrahydrofuran; mineral oil / 0.5 h / 0 °C / Inert atmosphere
10.2: 1 h / 20 °C / Inert atmosphere
With pyrrolidine; 1H-imidazole; Schwartz's reagent; chloro-trimethyl-silane; cerium(III) chloride heptahydrate; iodine; tert.-butyl lithium; sodium hydride; diisobutylaluminium hydride; propionic acid; triphenylphosphine; sodium iodide; In tetrahydrofuran; diethyl ether; ethanol; hexane; dichloromethane; water; dimethyl sulfoxide; isopropyl alcohol; acetonitrile; mineral oil; pentane; benzene; 9.3: |Suzuki-Miyaura Coupling;
DOI:10.1002/anie.201400305
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