HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115872Generated: October 31, 2026
Potassium Carbonate → HCID 59427967, compound
https://huagongshe.com/reaction/2115872
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,3-Propanediamine, N1,N1,N3-trimethyl- | HCID 78302 | — |
| Reactant | 3-Chloro-4-fluoro-5-nitrobenzotrifluoride | HCID 2736565 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59427967 | HCID 59427967 | — |
Reaction Steps
A heterogeneous mixture of 1-chloro-2-fluoro-3-nitro-5-(trifluoromethyl)benzene (1.25 mL, 8.2 mmol), K2CO3 (3.44 g, 24.6 mmol), N1,N1,N3-trimethylpropane-1,3-diamine (1.26 mL, 8.61 mmol) and THF were allowed to stir at RT for 45 min. The THF was removed under reduced pressure and reconstituted in EtOAc (50 ml). The organic layer was washed with water (20 ml), brine (20 ml), dried over anhydrous sodium sulfate, filtered and concentrated to an oil. The concentrated oil was taken up in EtOH (20 ml) to which Raney nickel (2.5 g wet, washed) was added. The reduction was monitored and after 1 h, another portion of Raney nickel (3.8 g, wet, washed) was added. The reaction was allowed to stir for an additional 30 min., and filtered through Celite, washed with EtOH (10 mL) and concentrated. The crude residue was purified via flash chromatography (silica gel, gradient elution 0 to 25% MeOH in CH2Cl2) to afford 6-chloro-N1-(3-(dimethylamino)propyl)-N1-methyl-4-(trifluoromethyl)benzene-1,2-diamine as a yellow oil. MS m/z=310.1 [M+H]+. Calc'd for C13H19ClF3N3: 309.8.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07435823B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-0c647f16f7e74af89039fede96eda6f1 |
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| Source note | uspto-grants-2008_10 |
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