HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410285Generated: October 28, 2026
Hydrochloric Acid → 1-N,1-N-diethyl-4-(trifluoromethyl)benzene-1,2-diamine
https://huagongshe.com/reaction/2410285
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N,N-Diethyl-2-nitro-4-(trifluoromethyl)aniline | HCID 23149637 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-N,1-N-diethyl-4-(trifluoromethyl)benzene-1,2-diamine | HCID 4962171 | 64.8% |
Reaction Steps
Concentrated hydrochloric acid (1.00 ml, 12.0 mmol) and anhydrous tin dichloride (908 mg, 4.78 mmol) were sequentially added at 0° C. to a methanol (5 ml) solution of 1-diethylamino-2-nitro-4-(trifluoromethyl)benzene (251 mg, 0.957 mmol), obtained as described in Referential Example 6-1. The resulting mixture was warmed to room temperature and stirred for 22 hours. A saturated solution of sodium hydrogen carbonate was added to the mixture, and the resulting mixture was extracted three times with ethyl acetate. The obtained organic layer was washed with a saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (20 g, hexane/ethyl acetate=20/1-10/1). Thus, 2-amino-1-diethylamino-4-(trifluoromethyl)benzene (144 mg, 64.7%) was yielded as a colorless oily material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08816089B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-858d922141b04e34a3c19fc4e37a9fd4 |
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| Source note | uspto-grants-2014_08 |
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