Technology Process of 2-(diisopropylcarbamoyl)benzene-1,4-diol
There total 14 articles about 2-(diisopropylcarbamoyl)benzene-1,4-diol 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
boron tribromide-dimethyl sulfide complex;
In
dichloromethane;
for 6h;
Heating;
DOI:10.1039/b004682p
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: 85 percent / pyridine
2.1: sec-butyllithium; TMEDA / tetrahydrofuran; hexane / -78 °C
2.2: 91 percent / tetrahydrofuran; hexane / 15 h / -78 - 20 °C
3.1: 60 percent / boron tribromide dimethylsulfide complex / CH2Cl2 / 6 h / Heating
With
pyridine; boron tribromide-dimethyl sulfide complex; N,N,N,N,-tetramethylethylenediamine; sec.-butyllithium;
In
tetrahydrofuran; hexane; dichloromethane;
1.1: Acylation / 2.1: Metallation / 2.2: Rearrangement / 3.1: Demethylation;
DOI:10.1039/b004682p
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: 92 percent / pyridine
2.1: sec-butyllithium; TMEDA / tetrahydrofuran; hexane / -78 °C
2.2: 71 percent / tetrahydrofuran; hexane / 15 h / -78 - 20 °C
3.1: n-butyllithium / tetrahydrofuran; hexane / 0 °C
3.2: 93 percent / tetrahydrofuran; hexane / 0 - 20 °C
4.1: LDA / tetrahydrofuran; hexane / 1 h / -78 °C
4.2: 32 percent Spectr. / aq. NH4Cl / tetrahydrofuran; hexane / -78 - 20 °C
5.1: 60 percent / boron tribromide dimethylsulfide complex / CH2Cl2 / 6 h / Heating
With
pyridine; n-butyllithium; boron tribromide-dimethyl sulfide complex; N,N,N,N,-tetramethylethylenediamine; sec.-butyllithium; lithium diisopropyl amide;
In
tetrahydrofuran; hexane; dichloromethane;
1.1: Acylation / 2.1: Metallation / 2.2: Rearrangement / 3.1: Metallation / 3.2: Esterification / 4.1: Metallation / 4.2: Hydrolysis / 5.1: Demethylation;
DOI:10.1039/b004682p