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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623932Generated: October 29, 2026

Hydroxylamine → Methyl 3-(4-{5-[amino(hydroxyimino)methyl]pyridin-2-yl}phenoxy)-2,2-dimethylpropanoate

https://huagongshe.com/reaction/623932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxylamineHCID 787—
ReactantMethanolHCID 887—
ReactantMethyl 3-[4-(5-cyanopyridin-2-yl)-phenoxy]-2,2-dimethylpropanoateHCID 67973192—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-(4-{5-[amino(hydroxyimino)methyl]pyridin-2-yl}phenoxy)-2,2-dimethylpropanoateHCID 8669818587.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

50% Aqueous hydroxylamine solution (40 g) was added to a methanol (100 mL) and tetrahydrofuran (100 mL) solution containing methyl 3-[4-(5-cyanopyridin-2-yl)-phenoxy]-2,2-dimethylpropanoate (6.0 g), and the mixture was stirred at 80° C. for 4 hours. After cooling the reaction mixture to room temperature, the mixture was concentrated under reduced pressure. To the obtained residue were added ethyl acetate and water, and the liquids were separated. The organic layer was separated, washed with water, and dried over anhydrous sodium sulfate. Ether was added to the solid residue obtained by concentrating the mixture under reduced pressure to pulverize the same, and the solid was collected by filtration and dried to obtain methyl 3-(4-{5-[amino(hydroxyimino)methyl]pyridin-2-yl}phenoxy)-2,2-dimethylpropanoate (5.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09302996B2
Source datasetuspto-grants-2016_04
ORD IDord-aeb11c8cd2da4f668149bca2c8a08711
Source noteuspto-grants-2016_04