Technology Process of C15H8(2)H5N
There total 5 articles about C15H8(2)H5N 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
tributylphosphine; di-isopropyl azodicarboxylate;
In
acetonitrile;
at 20 ℃;
for 2h;
DOI:10.1021/ja058026j
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 0.168 g / mCPBA; NaHCO3 / CH2Cl2 / 0 °C
2: 102 mg / BF3*OEt2 / diethyl ether / 0.02 h / 20 °C
3: NaOAc; NH2OH*HCl / methanol; H2O / 4 h / 20 °C
4: DIAD; tri-n-butylphosphine / acetonitrile / 2 h / 20 °C
With
tributylphosphine; di-isopropyl azodicarboxylate; boron trifluoride diethyl etherate; hydroxylamine hydrochloride; sodium acetate; sodium hydrogencarbonate; 3-chloro-benzenecarboperoxoic acid;
In
methanol; diethyl ether; dichloromethane; water; acetonitrile;
DOI:10.1021/ja058026j
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 102 mg / BF3*OEt2 / diethyl ether / 0.02 h / 20 °C
2: NaOAc; NH2OH*HCl / methanol; H2O / 4 h / 20 °C
3: DIAD; tri-n-butylphosphine / acetonitrile / 2 h / 20 °C
With
tributylphosphine; di-isopropyl azodicarboxylate; boron trifluoride diethyl etherate; hydroxylamine hydrochloride; sodium acetate;
In
methanol; diethyl ether; water; acetonitrile;
DOI:10.1021/ja058026j