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C15H17BrO2

Base Information Edit
C<sub>15</sub>H<sub>17</sub>BrO<sub>2</sub>

Synonyms:C15H17BrO2

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of C15H17BrO2 Edit
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Technology Process of C15H17BrO2

There total 1 articles about C15H17BrO2 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 toluene-4-sulfonic acid; In toluene; for 5h; Reflux; Dean-Stark;
DOI:10.1002/anie.201309521
Guidance literature:
ethyl 2-(2-tosylhydrazono)propanoate; With tris-(dibenzylideneacetone)dipalladium(0); lithium tert-butoxide; XPhos; In 1,4-dioxane; for 0.166667h; Inert atmosphere;
C15H17BrO2; In 1,4-dioxane; at 110 ℃; for 5h; Inert atmosphere;
DOI:10.1002/anie.201309521
Guidance literature:
Multi-step reaction with 4 steps
1.1: XPhos; tris-(dibenzylideneacetone)dipalladium(0); lithium tert-butoxide / 1,4-dioxane / 0.17 h / Inert atmosphere
1.2: 5 h / 110 °C / Inert atmosphere
2.1: lithium hydroxide / tetrahydrofuran; water / 5 h / 60 °C
3.1: triethylamine; hydrogen; C38H39IrNOP(1+)*C32H12BF24(1-) / dichloromethane / 10 h / 20 °C / 22801.5 Torr / Inert atmosphere; Glovebox; Autoclave
4.1: hydrogen; C38H39IrNOP(1+)*C32H12BF24(1-) / dichloromethane / 10 h / 20 °C / 22801.5 Torr / Inert atmosphere; Glovebox; Autoclave
With tris-(dibenzylideneacetone)dipalladium(0); C38H39IrNOP(1+)*C32H12BF24(1-); hydrogen; triethylamine; lithium hydroxide; lithium tert-butoxide; XPhos; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water;
DOI:10.1002/anie.201309521
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