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2-[(E)-but-2-en-1-yloxy]-6-methyl-4-[(E)-3-(propionyloxy)prop-1-en-1-yl]phenyl pivalate

Base Information
  • Chemical Name:2-[(E)-but-2-en-1-yloxy]-6-methyl-4-[(E)-3-(propionyloxy)prop-1-en-1-yl]phenyl pivalate
  • CAS No.:1414861-35-0
  • Molecular Formula:C22H30O5
  • Molecular Weight:374.477
  • Hs Code.:
2-[(E)-but-2-en-1-yloxy]-6-methyl-4-[(E)-3-(propionyloxy)prop-1-en-1-yl]phenyl pivalate

Synonyms:2-[(E)-but-2-en-1-yloxy]-6-methyl-4-[(E)-3-(propionyloxy)prop-1-en-1-yl]phenyl pivalate

Suppliers and Price of 2-[(E)-but-2-en-1-yloxy]-6-methyl-4-[(E)-3-(propionyloxy)prop-1-en-1-yl]phenyl pivalate
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Chemical Property of 2-[(E)-but-2-en-1-yloxy]-6-methyl-4-[(E)-3-(propionyloxy)prop-1-en-1-yl]phenyl pivalate
Chemical Property:
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Technology Process of 2-[(E)-but-2-en-1-yloxy]-6-methyl-4-[(E)-3-(propionyloxy)prop-1-en-1-yl]phenyl pivalate

There total 8 articles about 2-[(E)-but-2-en-1-yloxy]-6-methyl-4-[(E)-3-(propionyloxy)prop-1-en-1-yl]phenyl pivalate 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 potassium carbonate; palladium diacetate; In benzene; for 24h; Inert atmosphere; Reflux;
DOI:10.1055/s-0032-1316643
Guidance literature:
Multi-step reaction with 4 steps
1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 19 h / 0 - 20 °C / Inert atmosphere
2: acetyl chloride / methanol; dichloromethane / 24 h / 20 °C / Inert atmosphere
3: dmap; triethylamine / dichloromethane / 1.5 h / 20 °C / Inert atmosphere
4: potassium carbonate; palladium diacetate / benzene / 24 h / Inert atmosphere; Reflux
With dmap; di-isopropyl azodicarboxylate; potassium carbonate; palladium diacetate; triethylamine; acetyl chloride; triphenylphosphine; In tetrahydrofuran; methanol; dichloromethane; benzene; 4: |Heck Reaction;
DOI:10.1055/s-0032-1316643
Guidance literature:
Multi-step reaction with 3 steps
1: acetyl chloride / methanol; dichloromethane / 24 h / 20 °C / Inert atmosphere
2: dmap; triethylamine / dichloromethane / 1.5 h / 20 °C / Inert atmosphere
3: potassium carbonate; palladium diacetate / benzene / 24 h / Inert atmosphere; Reflux
With dmap; potassium carbonate; palladium diacetate; triethylamine; acetyl chloride; In methanol; dichloromethane; benzene; 3: |Heck Reaction;
DOI:10.1055/s-0032-1316643
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