HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370973Generated: October 30, 2026
alpha-Bromo-o-fluorotoluene → Ethyl (2-chloro-5-(4-(((2-fluorobenzyl)(2-methyl-3-nitrophenyl)amino)methyl)phenoxy)phenoxy)acetate
https://huagongshe.com/reaction/1370973
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | alpha-Bromo-o-fluorotoluene | HCID 67968 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 86759033 | HCID 86759033 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl (2-chloro-5-(4-(((2-fluorobenzyl)(2-methyl-3-nitrophenyl)amino)methyl)phenoxy)phenoxy)acetate | HCID 86586239 | — |
Reaction Steps
The product from Example 306A (86 mg, 0.18 mmoles) in anhydrous dimethylformamide (1 mL) was treated with Hunig's base (0.107 mL, 0.5 mmoles) and 1-(bromomethyl)-2-fluorobenzene (0.198 mL, 0.9 mmoles) in anhydrous dimethylformamide (1 mL) and heated at 90° C. for 72 hours. The reaction was diluted with ether, washed with saturated NH4Cl, water, brine, dried (Na2SO4), filtered, and filtrate concentrated under reduced pressure. The residue purified by using ethyl acetate and hexane gradient on 10 g silica column to provide the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06583180B2 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-bef470ae371b40938e2750ee2dc6ad19 |
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| Source note | uspto-grants-2003_06 |
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