HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404840Generated: October 31, 2026
Dimethyl Sulfoxide → HCID 86700483, compound
https://huagongshe.com/reaction/1404840
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Bromobenzylamine | HCID 77571 | — |
| Reactant | 2,3-Difluoro-6-nitroaniline | HCID 2737028 | — |
| Catalyst | Iodine | HCID 807 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86700483 | HCID 86700483 | 93.1% |
Reaction Steps
A round bottom flask was charged with 2,3-difluoro-6-nitroaniline (0.50 g, 2.87 mmol, 1.00 equiv.) and 4-bromobenzylamine (0.959 g, 5.15 mmol, 1.80 equiv.). Dimethyl sulfoxide (2.5 mL) was then added flowed by Et3N (0.968 mL, 6.88 mmol, 2.40 equiv.) and I2 (catalytic, 10 mg). The reaction mixture was heated to 120° C. and stirred for 3 h. The reaction mixture was then cooled to ambient temperature, diluted with water (75 mL) and extracted with Ethyl acetate (2×60 mL). The organic layer was dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure to give crude material, which was purified by silica gel column chromatography (10% ethyl acetate/hexane) to afford compound 3 as the desired product (0.869 g, 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916133B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-7525e736b3a34eaeb8f5998af24c6023 |
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| Source note | uspto-grants-2014_12 |
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