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di-t-butyl 5-trifluoromethyl-5,8-dideazaisofolate

Base Information Edit
  • Chemical Name:di-t-butyl 5-trifluoromethyl-5,8-dideazaisofolate
  • CAS No.:133116-90-2
  • Molecular Formula:C30H36F3N5O6
  • Molecular Weight:619.641
  • Hs Code.:
  • Mol file:133116-90-2.mol
di-t-butyl 5-trifluoromethyl-5,8-dideazaisofolate

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Chemical Property of di-t-butyl 5-trifluoromethyl-5,8-dideazaisofolate Edit
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Technology Process of di-t-butyl 5-trifluoromethyl-5,8-dideazaisofolate

There total 6 articles about di-t-butyl 5-trifluoromethyl-5,8-dideazaisofolate 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 4 steps
1: 34 percent / dimethylformamide / 35 h / Heating
2: 61 percent / 98 percent sulfuric acid, 90 percent nitric acid / 1) 0 deg C, 30 min; 2) RT, 24 h
3: 69 percent / H2 / 10 percent palladium charcoal / dimethylformamide; 2-methoxy-ethanol / 0.5 h / 2327.2 Torr
4: 1) dimethylformamide, glacial acetic acid, 3 Angstroem molecular sieves; 2) borane-t-butylamine complex / 1) RT, 6 h then 70 deg C, 20 h; 2) RT, 2 h then 70 deg C, 18 h
With 3 A molecular sieve; sulfuric acid; hydrogen; nitric acid; borane tert-butylamine; acetic acid; N,N-dimethyl-formamide; palladium on activated charcoal; In 2-methoxy-ethanol; N,N-dimethyl-formamide;
DOI:10.1002/jhet.5570270746
Guidance literature:
Multi-step reaction with 5 steps
1: 48 percent / monoperphthalic acid / diethyl ether; tetrahydrofuran / 5 h / 0 °C
2: 34 percent / dimethylformamide / 35 h / Heating
3: 61 percent / 98 percent sulfuric acid, 90 percent nitric acid / 1) 0 deg C, 30 min; 2) RT, 24 h
4: 69 percent / H2 / 10 percent palladium charcoal / dimethylformamide; 2-methoxy-ethanol / 0.5 h / 2327.2 Torr
5: 1) dimethylformamide, glacial acetic acid, 3 Angstroem molecular sieves; 2) borane-t-butylamine complex / 1) RT, 6 h then 70 deg C, 20 h; 2) RT, 2 h then 70 deg C, 18 h
With monoperoxyphthalic acid; 3 A molecular sieve; sulfuric acid; hydrogen; nitric acid; borane tert-butylamine; acetic acid; N,N-dimethyl-formamide; palladium on activated charcoal; In tetrahydrofuran; diethyl ether; 2-methoxy-ethanol; N,N-dimethyl-formamide;
DOI:10.1002/jhet.5570270746
Guidance literature:
Multi-step reaction with 5 steps
1: 98 percent / dimethylacetamide / 5 h / 128 - 130 °C
2: 94 percent / 1N aq. sodium hydroxide / 5 h / Heating
3: 61 percent / 98 percent sulfuric acid, 90 percent nitric acid / 1) 0 deg C, 30 min; 2) RT, 24 h
4: 69 percent / H2 / 10 percent palladium charcoal / dimethylformamide; 2-methoxy-ethanol / 0.5 h / 2327.2 Torr
5: 1) dimethylformamide, glacial acetic acid, 3 Angstroem molecular sieves; 2) borane-t-butylamine complex / 1) RT, 6 h then 70 deg C, 20 h; 2) RT, 2 h then 70 deg C, 18 h
With sodium hydroxide; ISOPROPYLAMIDE; 3 A molecular sieve; sulfuric acid; hydrogen; nitric acid; borane tert-butylamine; acetic acid; N,N-dimethyl-formamide; palladium on activated charcoal; In 2-methoxy-ethanol; N,N-dimethyl-formamide;
DOI:10.1002/jhet.5570270746
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