Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234817Generated: October 26, 2026

Water → 4-[4-(3,3-Dichloroprop-2-enyloxy)-2,6-dichlorophenoxy]butyl acetate

https://huagongshe.com/reaction/2234817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1,1,1,3-TetrachloropropaneHCID 14056—
Reactant4-(2,6-Dichloro-4-hydroxyphenoxy)butyl acetateHCID 57838141—
SolventDimethylformamideHCID 6228—
Product4-[4-(3,3-Dichloroprop-2-enyloxy)-2,6-dichlorophenoxy]butyl acetateHCID 1842950078.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 25.3 grams (0.086 mole) of 4-(2,6-dichloro-4-hydroxyphenoxy)butyl acetate in 250 mL of DMF was stirred, and 19.5 grams (0.1 mole) of 1,1,1,3-tetrachloropropane was added, followed by 18 grams (0.13 mole) of potassium carbonate. Upon completion of addition the reaction mixture was heated at 80° C. during a 17 hour period. After this time the reaction mixture was cooled to ambient temperature, stirred with 350 mL of water and extracted with four 150 mL portions of diethyl ether. The combined extracts were washed with two 100 mL portions of water, dried with sodium sulfate and filtered. The filtrate was concentrated under reduced pressure to a residue. The residue was purified with column chromatography on silica gel using 1:1 methylene chloride:hexane as an eluant. The appropriate fractions were combined and concentrated under reduced pressure, yielding 27.1 grams of the subject compound. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713970B2
Source datasetuspto-grants-2010_05
ORD IDord-62c566b93eea487293e5af09845f56a3
Source noteuspto-grants-2010_05