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(2R)-2-(2,2-dimethyl(4H-benzo[3,4-e]1,3-dioxin-6-yl))-N-(tert-butyl)-2-perhydro-2H-pyran-2-yloxyacetamide

Base Information Edit
  • Chemical Name:(2R)-2-(2,2-dimethyl(4H-benzo[3,4-e]1,3-dioxin-6-yl))-N-(tert-butyl)-2-perhydro-2H-pyran-2-yloxyacetamide
  • CAS No.:482308-28-1
  • Molecular Formula:C21H31NO5
  • Molecular Weight:377.481
  • Hs Code.:
  • Mol file:482308-28-1.mol
(2R)-2-(2,2-dimethyl(4H-benzo[3,4-e]1,3-dioxin-6-yl))-N-(tert-butyl)-2-perhydro-2H-pyran-2-yloxyacetamide

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Suppliers and Price of (2R)-2-(2,2-dimethyl(4H-benzo[3,4-e]1,3-dioxin-6-yl))-N-(tert-butyl)-2-perhydro-2H-pyran-2-yloxyacetamide
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (2R)-2-(2,2-dimethyl(4H-benzo[3,4-e]1,3-dioxin-6-yl))-N-(tert-butyl)-2-perhydro-2H-pyran-2-yloxyacetamide Edit
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Technology Process of (2R)-2-(2,2-dimethyl(4H-benzo[3,4-e]1,3-dioxin-6-yl))-N-(tert-butyl)-2-perhydro-2H-pyran-2-yloxyacetamide

There total 5 articles about (2R)-2-(2,2-dimethyl(4H-benzo[3,4-e]1,3-dioxin-6-yl))-N-(tert-butyl)-2-perhydro-2H-pyran-2-yloxyacetamide 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:
Multi-step reaction with 3 steps
1.1: 88 percent / TsOH / CH2Cl2 / 4 h / 20 °C
2.1: trifluoroacetic anhydride; pyridine / CH2Cl2; tetrahydrofuran / 0.25 h / 0 °C
2.2: LiOH*H2O / CH2Cl2; tetrahydrofuran; H2O / 3 h / 0 - 20 °C
3.1: 57 percent / AgOCOCF3 / acetonitrile / 96 h / 40 °C
With pyridine; silver trifluoroacetate; toluene-4-sulfonic acid; trifluoroacetic anhydride; In tetrahydrofuran; dichloromethane; acetonitrile; 2.1: Pummerer reaction;
DOI:10.1021/jo026410i
Guidance literature:
Multi-step reaction with 4 steps
1.1: 89 percent / NaHMDS / pyridine; tetrahydrofuran / 2 h / 0 °C
2.1: 88 percent / TsOH / CH2Cl2 / 4 h / 20 °C
3.1: trifluoroacetic anhydride; pyridine / CH2Cl2; tetrahydrofuran / 0.25 h / 0 °C
3.2: LiOH*H2O / CH2Cl2; tetrahydrofuran; H2O / 3 h / 0 - 20 °C
4.1: 57 percent / AgOCOCF3 / acetonitrile / 96 h / 40 °C
With pyridine; sodium hexamethyldisilazane; silver trifluoroacetate; toluene-4-sulfonic acid; trifluoroacetic anhydride; In tetrahydrofuran; pyridine; dichloromethane; acetonitrile; 3.1: Pummerer reaction;
DOI:10.1021/jo026410i
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