HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992797Generated: October 30, 2026
1,2-Dichloroethane → HCID 86761041, compound
https://huagongshe.com/reaction/1992797
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | 4-(Trifluoromethoxy)aniline | HCID 600848 | — |
| Reactant | HCID 68428139 | HCID 68428139 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86761041 | HCID 86761041 | — |
Reaction Steps
To a solution of the intermediate from step D (0.1 g, 0.41 mmol) in DMF (2 mL) was added 4-trifluoromethoxy aniline (83 μL, 0.61 mmol), DIEA (215 μL, 1.23 mmol), HOAt (0.08 g, 0.61 mmol) and EDC (0.118 g, 0.61 mmol). The reaction was heated at 50° C. for 3 hours. The reaction was diluted with ethyl acetate, washed with 1N HCl , saturated NaHCO3, and saturated NaCl solutions. The organic layer was dried over anhydrous Na2SO4, filtered and concentrated in vacuo. The residue was purified by flash chromatography using 30% ethyl acetate hexanes. 1H NMR (DMSO, 500 MHz): 10.34 (bs, 1H), 7.93 (d, J=5.9 Hz, 2H), 7.8 (bm, 2H), 7.44 (bs, 1H), 7.37 (bd, J=8.0 Hz, 2H). LC-MS=3.76 min; (M+H)=402.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07649009B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-01ded6e49f1047839ba094d839d771ac |
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| Source note | uspto-grants-2010_01 |
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