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β-hydroxy-β-(2-methoxyphenyl)-2-methoxybenzenepropanenitrile

Base Information
  • Chemical Name:β-hydroxy-β-(2-methoxyphenyl)-2-methoxybenzenepropanenitrile
  • CAS No.:120553-98-2
  • Molecular Formula:C17H17NO3
  • Molecular Weight:283.327
  • Hs Code.:
β-hydroxy-β-(2-methoxyphenyl)-2-methoxybenzenepropanenitrile

Synonyms:β-hydroxy-β-(2-methoxyphenyl)-2-methoxybenzenepropanenitrile

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Chemical Property of β-hydroxy-β-(2-methoxyphenyl)-2-methoxybenzenepropanenitrile
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Technology Process of β-hydroxy-β-(2-methoxyphenyl)-2-methoxybenzenepropanenitrile

There total 1 articles about β-hydroxy-β-(2-methoxyphenyl)-2-methoxybenzenepropanenitrile 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 n-butyllithium; diisopropylamine; Yield given. Multistep reaction; 1.) THF, hexane, -70 deg C, 5 min, 2.) THF, -70 -> -35 deg C, 15 min;
DOI:10.1021/jm00128a026
Guidance literature:
With pyridine; thionyl chloride; for 2h; Ambient temperature;
DOI:10.1021/jm00128a026
Guidance literature:
Multi-step reaction with 5 steps
1: 71.5 percent / SOCl2, pyridine / 2 h / Ambient temperature
2: 1.) DIBAH, 2.) 5percent H2SO4 / 1.) toluene, hexane, a) -40 deg C, 1 h, b) -40 -> -12 deg C, 1 h, 2.) a) -10 deg C, b) 40 deg C, 2.5 h
3: 2.) NaOH / 1.) CH2Cl2, room temperature, 3 d, 2.) MeOH, H2O, reflux, 30 min
4: 88 percent / DCC / CH2Cl2 / 1.) 0-5 deg C, 60 min, 2.) room temperature, overnight
5: 81 percent / tetrahydrofuran / 1.) room temperature, overnight, 2.) reflux, 3 h
With pyridine; sodium hydroxide; thionyl chloride; sulfuric acid; diisobutylaluminium hydride; dicyclohexyl-carbodiimide; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm00128a026
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