Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Iodoaniline | HCID 12271 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,4,4,6-Tetrabromocyclohexa-2,5-dienone | HCID 88433 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Bromo-3-iodoaniline | HCID 14548337 | — |
Reaction Steps
To a solution of 3-iodoaniline (12 mL, 100 mmol) in 400 mL CH2Cl2 at −10° C. was added in portions 2,4,4,6-tetrabromo-2,5-cyclohexadienone (45.1 g, 110 mmol) while maintaining an internal temperature of −10° C. After stirring for 4 hours, 150 mL of 1N NaOH was added, and the product was extracted with CH2Cl2. The combined extracts were washed with water and then brine and dried over Na2SO4. After concentration in vacuo the crude product was recrystallized with 2:1 hexanes:toluene to yield the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08168815B2 |
|---|
| Source dataset | uspto-grants-2012_05 |
|---|
| ORD ID | ord-d1a5f65a0fa542e1a847c8dd584d7b33 |
|---|
| Source note | uspto-grants-2012_05 |
|---|