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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343284Generated: October 30, 2026

Ethyl Acetate → Methyl 2-[5-chloro-2-[4-(4-chloro-5-difluoromethoxy-1-methylpyrazol-3-yl)phenoxymethyl]phenoxy]propanoate

https://huagongshe.com/reaction/343284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 2-(2-chloromethyl-5-chlorophenoxy)propionateHCID 53768369—
Reactant4-(4-Chloro-5-difluoromethoxy-1-methylpyrazol-3-yl)phenolHCID 136168448—
SolventDimethylformamideHCID 6228—
SolventHeptaneHCID 8900—
ProductMethyl 2-[5-chloro-2-[4-(4-chloro-5-difluoromethoxy-1-methylpyrazol-3-yl)phenoxymethyl]phenoxy]propanoateHCID 6770335445.2%

Reaction Steps

This compound was prepared in a manner analogous to that of Step I of Example 1, using 0.82 gram (0.0030 mole) of 4-(4-chloro-5-difluoromethoxy-1-methylpyrazol-3-yl)phenol, 0.95 gram (0.0036 mole) of methyl 2-(5-chloro-2-chloromethylphenoxy)propanoate (prepared in Steps A through D of this Example), and 0.62 gram (0.0045 mole) of potassium carbonate in N,N-dimethylformamide. The crude reaction product was subjected to column chromatography on silica gel, using 1:4 ethyl acetate and heptane as the eluant. The product-containing fractions were combined and concentrated under reduced pressure to an oil. The oil was triturated with heptane, yielding 0.68 gram of title compound, mp 61-64° C. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05861359
Source datasetuspto-grants-1999_01
ORD IDord-dbb49b81868f4a568ef1f1c3012fc1b2
Source noteuspto-grants-1999_01