HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → Ethyl 4-amino-3-bromo-5-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Benzoic acid, 4-amino-3-nitro-, ethyl ester | HCID 3018687 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 4-amino-3-bromo-5-nitrobenzoate | HCID 3019079 | 94% |
Reaction Steps
To a solution of ethyl 4-amino-3-nitrobenzoate (D212) (21.0 g, 100 mmol, 1 equiv) in CH2Cl2 (500 ml) at room temperature was added bromine (6.7 ml, 130 mmol, 1.3 equiv) and the resulting mixture was refluxed for 4 h then bromine (2 ml, 40 mmol, 0.4 equiv) was added and the resulting mixture refluxed for another 3 h then cooled to room temperature. The organic phase was washed twice with a 10% aqueous Na2S2O3 solution and twice with H2O, dried over MgSO4 and concentrated in vacuo to give ethyl 4-amino-3-bromo-5-nitrobenzoate (D213) (27.1 g, 94%) as a yellow solid which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07253198B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-79ed2912926646e2a2f3706c971546e4 |
| Source note | uspto-grants-2007_08 |