HuagongsheHuagongshe Chemistry Print Report · For research reference only
Stannous Chloride → 4,5-Dichloro-2-fluoroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1,2-Dichloro-4-fluoro-5-nitrobenzene | HCID 533951 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4,5-Dichloro-2-fluoroaniline | HCID 223091 | — |
Reaction Steps
Tin (II) chloride dehydrate (27.0 g, 119.6 mmol) was dissolved in ethanol and 1,2-dichloro-4-fluoro-5-nitrobenzene (5.0 g, 23.8 mmol) was added dropwise. Temperature rose to near reflux during the addition and was complete upon cooling. The reaction mixture was carefully added to saturated aqueous sodium bicarbonate and then extracted with ethyl acetate. The organic phase was washed several more times with water, dried, filtered and concentrated to give the title compound as a yellow solid: 1H NMR (CDCl3): δ 7.17 (d, 1H), 6.84 (d, 1H), 3.78 (br s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08357633B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-62f326a4b8e84982b3ae0cc9b6ed6bce |
| Source note | uspto-grants-2013_01 |