Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3,5-diiodonitrobenzene | HCID 12134256 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3,5-DIIODOANILINE | HCID 12134254 | 70% |
Reaction Steps
To a suspension of 3,5-diiodonitrobenzene (10 g, 26.7 mmol) in anhydrous EtOH (100 mL) was added SnCl2.2H2O (30 g, 133.6 mmol). The reaction mixture was brought to boil and a solution of NaBH4 (508 mg, 13.4 mmol) in EtOH (50 mL) was added slowly then stirred at reflux for 1 h. After the reaction was cooled down to 0° C., the mixture was neutralized with a solution of 3M NaOH (200 mL). The aniline derivative was extracted with chloroform, dried over Na2SO4 and evaporated under reduced pressure to afford 6.4 g of 3,5-diiodoaniline 11(70%) as a white solid. HR-ES(+): calculated for C6H5I2N [M] 345.8584, found 345.8583.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093385B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-f5c19a811d344ebba07641504564eeb7 |
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| Source note | uspto-grants-2012_01 |
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