Technology Process of 1,9-Phenanthroline-4-carboxylic acid,
2-[(4-chlorophenyl)methyl]-7,8,9,10-tetrahydro-3-hydroxy-9-(1-methyleth
yl)-
There total 9 articles about 1,9-Phenanthroline-4-carboxylic acid,
2-[(4-chlorophenyl)methyl]-7,8,9,10-tetrahydro-3-hydroxy-9-(1-methyleth
yl)- 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
sodium cyanoborohydride; acetic acid; triethylamine;
In
methanol;
at 25 ℃;
DOI:10.1021/jm060631p
- Guidance literature:
-
Multi-step reaction with 5 steps
1: aq. NaHCO3 / CH2Cl2 / 0.5 h / 0 °C
2: NH2OH*HCl; Na2SO4; aq. HCl / CH2Cl2 / 55 °C
3: H2SO4 / 55 - 80 °C
4: 16 percent / aq. NaOH / ethanol / 2 h / Heating
5: 32 percent / NaBH3CN; Et3N; AcOH / methanol / 25 °C
With
hydrogenchloride; sodium hydroxide; sulfuric acid; hydroxylamine hydrochloride; sodium cyanoborohydride; sodium hydrogencarbonate; acetic acid; sodium sulfate; triethylamine;
In
methanol; ethanol; dichloromethane;
2: Sandmeyer reaction / 4: Pfitzinger reaction;
DOI:10.1021/jm060631p
- Guidance literature:
-
Multi-step reaction with 4 steps
1: NH2OH*HCl; Na2SO4; aq. HCl / CH2Cl2 / 55 °C
2: H2SO4 / 55 - 80 °C
3: 16 percent / aq. NaOH / ethanol / 2 h / Heating
4: 32 percent / NaBH3CN; Et3N; AcOH / methanol / 25 °C
With
hydrogenchloride; sodium hydroxide; sulfuric acid; hydroxylamine hydrochloride; sodium cyanoborohydride; acetic acid; sodium sulfate; triethylamine;
In
methanol; ethanol; dichloromethane;
1: Sandmeyer reaction / 3: Pfitzinger reaction;
DOI:10.1021/jm060631p