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 | 61.9% |
Reaction Steps
A mixture of 61.5 g (0.164M) of 3,5-diiodonitrobenzene and 111.1 g (0.4924M) of stannous chloride in 900 mL of ethanol was heated to reflux 1.5 hrs under nitrogen. The reaction mixture was cooled and most of the solvent was removed in vacuo. The residue was partitioned between ethyl acetate and excess ice-cold 5N sodium hydroxide and ice. The organic phase was separated, washed with sat'd sodium chloride solution, and dried over anhyd. magnesium sulfate. Solvent removal afforded a crude oil which was purified on silica gel using 8:1:1 mixture of hexane:methylene chloride:ethyl acetate to give 35 g of 3,5-diiodoaniline as a light tan colored solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05292879 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-410acc0ad4a048879d6105580d543ac9 |
| Source note | uspto-grants-1994_03 |