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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactantalpha-Bromo-o-fluorotolueneHCID 67968—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86759033HCID 86759033—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductEthyl (2-chloro-5-(4-(((2-fluorobenzyl)(2-methyl-3-nitrophenyl)amino)methyl)phenoxy)phenoxy)acetateHCID 86586239—

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583180B2
Source datasetuspto-grants-2003_06
ORD IDord-bef470ae371b40938e2750ee2dc6ad19
Source noteuspto-grants-2003_06