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methyl 15-(3-nitrophenyl)pentadec-12-enoate

Base Information
  • Chemical Name:methyl 15-(3-nitrophenyl)pentadec-12-enoate
  • CAS No.:121269-67-8
  • Molecular Formula:C22H33NO4
  • Molecular Weight:375.508
  • Hs Code.:
methyl 15-(3-nitrophenyl)pentadec-12-enoate

Synonyms:methyl 15-(3-nitrophenyl)pentadec-12-enoate

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Chemical Property of methyl 15-(3-nitrophenyl)pentadec-12-enoate
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Technology Process of methyl 15-(3-nitrophenyl)pentadec-12-enoate

There total 8 articles about methyl 15-(3-nitrophenyl)pentadec-12-enoate 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 tert-butylate; In dichloromethane; for 3h; Ambient temperature;
DOI:10.1021/jm00129a014
Guidance literature:
Multi-step reaction with 3 steps
1: H2SO4 / 6 h / Heating
2: 68 percent / pyridinium chlorochromate (PCC) / CH2Cl2 / 2 h / Ambient temperature
3: 48 percent / KOt-Bu / CH2Cl2 / 3 h / Ambient temperature
With sulfuric acid; potassium tert-butylate; pyridinium chlorochromate; In dichloromethane;
DOI:10.1021/jm00129a014
Guidance literature:
Multi-step reaction with 5 steps
1: 71 percent / (H2NOH)2, H2SO4, H2NOSO3H, NaOH / H2O / 5.5 h / 10 °C / pH 6-7
2: 72 percent / BF3 / tetrahydrofuran / 2 h / Ambient temperature
3: 58 percent / PBr3, pyridine / benzene / 1) 0 deg C, 1 h, 2) 65 deg C, 5.5 h
4: 66 percent / acetonitrile / 44 h / Heating
5: 48 percent / KOt-Bu / CH2Cl2 / 3 h / Ambient temperature
With pyridine; sodium hydroxide; (H2NOH)2; sulfuric acid; boron trifluoride; potassium tert-butylate; phosphorus tribromide; hydroxylamine-O-sulfonic acid; In tetrahydrofuran; dichloromethane; water; acetonitrile; benzene;
DOI:10.1021/jm00129a014
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