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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611450Generated: November 2, 2026

Sodium Chloride → 1,3-Dichloro-2-(4-chlorobutoxy)-5-(phenylmethoxy)benzene

https://huagongshe.com/reaction/1611450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-4-chlorobutaneHCID 81364—
Reactant2,6-Dichloro-4-benzyloxyphenolHCID 12084170—
SolventDimethylformamideHCID 6228—
Product1,3-Dichloro-2-(4-chlorobutoxy)-5-(phenylmethoxy)benzeneHCID 2225712366.5%

Reaction Steps

A stirred solution of 7.5 grams (0.028 mole) of 2,6-dichloro-4-phenylmethoxyphenol (known compound) and 3 mL (0.030 mole) of 1-bromo-4-chlorobutane in 225 mL of DMF was cooled in an ice bath, and 5.8 grams (0.042 mole) of potassium carbonate was added. Upon completion of addition, the reaction mixture was allowed to warm to ambient temperature as it stirred for about 18 hours. The reaction mixture was then poured into 1000 mL of an aqueous solution saturated with sodium chloride. The mixture was extracted with four 150 mL portions of diethyl ether, and the combined extracts were washed with 50 mL of water. The organic layer was dried with sodium sulfate, filtered, and concentrated under reduced pressure to a residue. The residue was purified with column chromatography on silica gel using 1:3 methylene chloride:hexane as an eluant. The appropriate fractions were combined and concentrated under reduced pressure, yielding 6.7 grams of the subject compound. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06987194B2
Source datasetuspto-grants-2006_01
ORD IDord-25fa8971cf624895b91f31ac5155a455
Source noteuspto-grants-2006_01