HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446246Generated: October 29, 2026
Ethyl Acetate → 4-bromo-N1-(3-(dimethylamino)propyl)-N1-methylbenzene-1,2-diamine
https://huagongshe.com/reaction/446246
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 16109013 | HCID 16109013 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-bromo-N1-(3-(dimethylamino)propyl)-N1-methylbenzene-1,2-diamine | HCID 59427923 | — |
Reaction Steps
To N-(4-Bromo-2-nitro-phenyl)-N,N′,N′-trimethyl-propane-1,3-diamine (Example 619, Step 1) (0.54 g, 1.7 mmol) in 20 ml EtOH was added SnCl2 (0.51 g, 2.67 mmol). The mixture was sealed and was heated to 80° C. for 12 h. An additional amount of SnCl2 (0.51 g, 2.67 mmol) was added and heating continued for 12 h. The reaction was cooled to ambient temperature, and was poured into a mixture of EtOAc and saturated aqueous sodium bicarbonate. The mixture was filtered through celite, and the organic layer was removed. The aqueous layer was extracted twice with EtOAc, and the combined organic layers were dried with Na2SO4, filtered, and concentrated to give a cloudy oil. This material was filtered through silica gel with 90/10/1 dichloromethane/MeOH/conc. NH4OH and concentrated in vacuo to give the title compound as a red oil. MS (ES+): 285.9 (M+H)+. Calc'd for C12H20BrN3: 286.21.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08476434B2 |
|---|
| Source dataset | uspto-grants-2013_07 |
|---|
| ORD ID | ord-0003bf079656431baa5fc2cabd301833 |
|---|
| Source note | uspto-grants-2013_07 |
|---|