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2-diazo-3-phenylpropionic acid 3-phenylprop-2-ynyl ester

Base Information
  • Chemical Name:2-diazo-3-phenylpropionic acid 3-phenylprop-2-ynyl ester
  • CAS No.:187337-16-2
  • Molecular Formula:C18H14N2O2
  • Molecular Weight:290.321
  • Hs Code.:
2-diazo-3-phenylpropionic acid 3-phenylprop-2-ynyl ester

Synonyms:2-diazo-3-phenylpropionic acid 3-phenylprop-2-ynyl ester

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Chemical Property of 2-diazo-3-phenylpropionic acid 3-phenylprop-2-ynyl ester
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Technology Process of 2-diazo-3-phenylpropionic acid 3-phenylprop-2-ynyl ester

There total 3 articles about 2-diazo-3-phenylpropionic acid 3-phenylprop-2-ynyl ester 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 p-nitrobenzenesulfonyl azide; 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; at 0 ℃; for 0.166667h;
DOI:10.1021/jo991938h
Guidance literature:
Multi-step reaction with 3 steps
1.1: 92 percent / xylene / 2 h / 140 °C
2.1: NaH / tetrahydrofuran / 0.5 h / 25 °C
2.2: 91 percent / tetrahydrofuran / 4 h / 60 °C
3.1: 72 percent / p-nitrobenzenesulfonyl azide; 1,8-diazabicyclo[5.4.0]undec-7-ene / CH2Cl2 / 0.17 h / 0 °C
With p-nitrobenzenesulfonyl azide; sodium hydride; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; dichloromethane; xylene; 1.1: Ring cleavage / 2.1: deprotonation / 2.2: Alkylation / 3.1: Diazotization;
DOI:10.1021/jo991938h
Guidance literature:
Multi-step reaction with 2 steps
1.1: NaH / tetrahydrofuran / 0.5 h / 25 °C
1.2: 91 percent / tetrahydrofuran / 4 h / 60 °C
2.1: 72 percent / p-nitrobenzenesulfonyl azide; 1,8-diazabicyclo[5.4.0]undec-7-ene / CH2Cl2 / 0.17 h / 0 °C
With p-nitrobenzenesulfonyl azide; sodium hydride; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; dichloromethane; 1.1: deprotonation / 1.2: Alkylation / 2.1: Diazotization;
DOI:10.1021/jo991938h
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