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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850154Generated: October 26, 2026

Water → Metabolite 10 of Picoxystrobin

https://huagongshe.com/reaction/850154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 2-[2-(chloromethyl)phenyl]acetateHCID 9855748—
ReactantHCID 178516021HCID 178516021—
CatalystSodium IodideHCID 5238—
Catalyst15-Crown-5HCID 36336—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
ProductMetabolite 10 of PicoxystrobinHCID 1086034483%

Reaction Steps

A mixture of 2-hydroxy-6-trifluoromethylpyridine (2.0 g, 12.3 mmol), sodium hydroxide (0.52 g, 12.9 mmol) and 15-crown-5 (1 drop) in dry toluene (25 ml) were stirred at reflux for 2 hours. The toluene was removed under reduced pressure and the white salt residue was dissolved in dry DMF (15 ml). Methyl 2-chloromethylphenylacetate (2.44 g, 12.3 mmol) in dry DMF (15 ml) was added dropwise along with sodium iodide (10 mg). The mixture was stirred at 75° C. for 2 hours, poured into water and extracted with diethyl ether. The ether extracts were washed with water, dried and the ether removed in vacuo leaving an oil which was purified by column chromatography (silica eluted with 10% ethyl acetate in hexane) to give methyl 2-(6-tri-fluoromethylpyrid-2-yloxymethyl)phenylacetate (3.3 g, 83%) (Compound No.5 in Table 1) as a yellow oil; 1H NMR (270 MHz)δ: 3.68(3H,s), 3.84(2H,s), 5.46(2H,s), 6.89(1H,d), 7,20-7.70(6H,m) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06015905
Source datasetuspto-grants-2000_01
ORD IDord-fc309df0347749e08d10bf07191036b3
Source noteuspto-grants-2000_01