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phenyl (2-hydroxy-3,5-dimethyl)phenoxyacetate

Base Information
  • Chemical Name:phenyl (2-hydroxy-3,5-dimethyl)phenoxyacetate
  • CAS No.:265983-72-0
  • Molecular Formula:C16H16O4
  • Molecular Weight:272.301
  • Hs Code.:
phenyl (2-hydroxy-3,5-dimethyl)phenoxyacetate

Synonyms:phenyl (2-hydroxy-3,5-dimethyl)phenoxyacetate

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Chemical Property of phenyl (2-hydroxy-3,5-dimethyl)phenoxyacetate
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Technology Process of phenyl (2-hydroxy-3,5-dimethyl)phenoxyacetate

There total 5 articles about phenyl (2-hydroxy-3,5-dimethyl)phenoxyacetate 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 hydrogen; palladium on activated charcoal; In tetrachloromethane; for 1h; under 2844.39 Torr; Title compound not separated from byproducts.;
DOI:10.1021/jo9915168
Guidance literature:
Multi-step reaction with 5 steps
1.1: 85 percent / KH / dimethylformamide / 12 h / 0 - 5 °C
2.1: mCPBA; CF3COOH / CH2Cl2 / 5 h / 0 - 5 °C
2.2: 81 percent / aq. KOH / methanol / 12 h
3.1: 90 percent / NaH / dimethylformamide / 12 h
4.1: 81 percent / 1,3-dicyclohexylcarbodiimide; pyridine / CH2Cl2 / 12 h / 20 °C
5.1: H2 / Pd/C / CCl4 / 1 h / 2844.39 Torr
With pyridine; hydrogen; potassium hydride; sodium hydride; 3-chloro-benzenecarboperoxoic acid; dicyclohexyl-carbodiimide; trifluoroacetic acid; palladium on activated charcoal; In tetrachloromethane; dichloromethane; N,N-dimethyl-formamide; 1.1: Alkylation / 2.1: Oxidation / 2.2: Hydrolysis / 3.1: Alkylation / 4.1: Condensation / 5.1: Hydrogenolysis;
DOI:10.1021/jo9915168
Guidance literature:
Multi-step reaction with 3 steps
1: 90 percent / NaH / dimethylformamide / 12 h
2: 81 percent / 1,3-dicyclohexylcarbodiimide; pyridine / CH2Cl2 / 12 h / 20 °C
3: H2 / Pd/C / CCl4 / 1 h / 2844.39 Torr
With pyridine; hydrogen; sodium hydride; dicyclohexyl-carbodiimide; palladium on activated charcoal; In tetrachloromethane; dichloromethane; N,N-dimethyl-formamide; 1: Alkylation / 2: Condensation / 3: Hydrogenolysis;
DOI:10.1021/jo9915168
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