HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,5-diiodonitrobenzene → 3,5-DIIODOANILINE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,5-diiodonitrobenzene | HCID 12134256 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3,5-DIIODOANILINE | HCID 12134254 | — |
Reaction Steps
A mixture of 61.5 G (0.164M) of 3,5-diiodonitrobenzene, from step (a), and 111.1 G (0.4924M) of stannous chloride in 900 ml of absolute ethanol was heated to reflux 1.5 hours under nitrogen. Most of the solvent was removed. The residue was stirred with ethylacetate, 5 normal sodium hydroxide and ice. Organic phase was separated and washed with saturated sodium chloride solution. After drying over anhydrous magnesium sulfate, solvent was removed to afford a crude oil, which was chromatographed on silica gel using 8:1:1 mixture of hexane:methylene chloride:ethyl acetate. The desired aniline was obtained as 35 G of light tan colored solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05256777 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-2304b7b89573467fbe4b84956bb03d49 |
| Source note | uspto-grants-1993_10 |