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1-O-(5'-carbomethoxypentyl)-2-tetrahydropyranyl-sn-3-glyceryl 2,2,2-trichloro-tert-butyl 1-N-triphenylmethylamino-1-carbomethoxy-2-propyl phosphate

Base Information Edit
  • Chemical Name:1-O-(5'-carbomethoxypentyl)-2-tetrahydropyranyl-sn-3-glyceryl 2,2,2-trichloro-tert-butyl 1-N-triphenylmethylamino-1-carbomethoxy-2-propyl phosphate
  • CAS No.:142350-49-0
  • Molecular Formula:C43H57Cl3NO11P
  • Molecular Weight:901.258
  • Hs Code.:
  • Mol file:142350-49-0.mol
1-O-(5'-carbomethoxypentyl)-2-tetrahydropyranyl-sn-3-glyceryl 2,2,2-trichloro-tert-butyl 1-N-triphenylmethylamino-1-carbomethoxy-2-propyl phosphate

Synonyms:1-O-(5'-carbomethoxypentyl)-2-tetrahydropyranyl-sn-3-glyceryl 2,2,2-trichloro-tert-butyl 1-N-triphenylmethylamino-1-carbomethoxy-2-propyl phosphate

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Chemical Property of 1-O-(5'-carbomethoxypentyl)-2-tetrahydropyranyl-sn-3-glyceryl 2,2,2-trichloro-tert-butyl 1-N-triphenylmethylamino-1-carbomethoxy-2-propyl phosphate Edit
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Technology Process of 1-O-(5'-carbomethoxypentyl)-2-tetrahydropyranyl-sn-3-glyceryl 2,2,2-trichloro-tert-butyl 1-N-triphenylmethylamino-1-carbomethoxy-2-propyl phosphate

There total 13 articles about 1-O-(5'-carbomethoxypentyl)-2-tetrahydropyranyl-sn-3-glyceryl 2,2,2-trichloro-tert-butyl 1-N-triphenylmethylamino-1-carbomethoxy-2-propyl phosphate 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 7 steps
1.1: HCl
2.1: 89 percent / BF3*OEt2 / CH2Cl2 / 4 h
3.1: 69 percent / pyridinium p-toluenesulfonate / CH2Cl2 / 4 h / 20 °C
4.1: 90 percent / molecular sieves 3A / acetonitrile / 36 h / 20 °C
5.1: 75 percent / potassium carbonate / methanol / 0.5 h / 0 °C
6.1: diisopropylethylamine / tetrahydrofuran / 0.25 h / -78 °C
6.2: 45 percent / tetrahydrofuran / -78 - 20 °C
7.1: 92 percent / hydrogen peroxide / H2O; CH2Cl2 / 2 h / 20 °C
With hydrogenchloride; 3 A molecular sieve; boron trifluoride diethyl etherate; dihydrogen peroxide; pyridinium p-toluenesulfonate; potassium carbonate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; dichloromethane; water; acetonitrile; 1.1: Esterification / 2.1: Ring cleavage / 3.1: Addition / 4.1: Acetoxylation / 5.1: Deacetylation / 6.1: phosphitylation; phosphorylation / 6.2: coupling; phosphorylation; phosphitylation / 7.1: Oxidation;
DOI:10.1021/jo990739v
Guidance literature:
Multi-step reaction with 6 steps
1.1: 89 percent / BF3*OEt2 / CH2Cl2 / 4 h
2.1: 69 percent / pyridinium p-toluenesulfonate / CH2Cl2 / 4 h / 20 °C
3.1: 90 percent / molecular sieves 3A / acetonitrile / 36 h / 20 °C
4.1: 75 percent / potassium carbonate / methanol / 0.5 h / 0 °C
5.1: diisopropylethylamine / tetrahydrofuran / 0.25 h / -78 °C
5.2: 45 percent / tetrahydrofuran / -78 - 20 °C
6.1: 92 percent / hydrogen peroxide / H2O; CH2Cl2 / 2 h / 20 °C
With 3 A molecular sieve; boron trifluoride diethyl etherate; dihydrogen peroxide; pyridinium p-toluenesulfonate; potassium carbonate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; dichloromethane; water; acetonitrile; 1.1: Ring cleavage / 2.1: Addition / 3.1: Acetoxylation / 4.1: Deacetylation / 5.1: phosphitylation; phosphorylation / 5.2: coupling; phosphorylation; phosphitylation / 6.1: Oxidation;
DOI:10.1021/jo990739v
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