HuagongsheHuagongshe Chemistry Print Report · For research reference only
Stannous Chloride → 5-bromo-N1-(3-methoxypropyl)benzene-1,2-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | (5-Bromo-2-nitrophenyl)(3-methoxypropyl)amine | HCID 65341496 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-bromo-N1-(3-methoxypropyl)benzene-1,2-diamine | HCID 65343412 | — |
Reaction Steps
78.57 g of tin(II) chloride are added to a solution of 21.01 g of (5-bromo-2-nitrophenyl)-(3-methoxypropyl)amine in 950 ml of ethanol. The reaction mixture is heated to reflux for 12 hours. The mixture is cooled to room temperature and concentrated by evaporation. The residue is treated with 2M NaOH until a pH of 11 has been attained. The mixture is extracted with tert-butyl methyl ether (3×). The combined organic phases are dried with sodium sulphate and concentrated by evaporation. The title compound is obtained as an orange oil from the residue. Rf=0.31 (1:1 EtOAc-heptane). Rt=3.06 (gradient I).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07851634B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-f2fd000caa8a44e0aaf3078c14ce78b0 |
| Source note | uspto-grants-2010_12 |