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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576153Generated: October 30, 2026

Hydrochloric Acid → HCID 56954313, compound

https://huagongshe.com/reaction/576153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium BicarbonateHCID 516892—
Reactant5,5,5-Trifluoro-4,4-dimethyl-3-oxopentanenitrileHCID 56954310—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 56954313HCID 5695431340.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of hydroxylamine, hydrochloride (3.10 g, 44.7 mmol) in H2O (25 mL) cooled to 0° C. was added NaHCO3 (3.94 g, 46.9 mmol) to adjust to pH=7.5. Then to the mixture was added a solution of 5,5,5-trifluoro-4,4-dimethyl-3-oxopentanenitrile (4 g, 22.33 mmol) in MeOH (25 mL). The mixture was stirred at 65° C. for 15 h. After cooled, the mixture was acidified with conc. HCl to pH=1.0 and then refluxed for 2 h. After cooling, the mixture was neutralized by 4 mol/L NaOH to pH=8.0. The mixture was extracted with DCM/MeOH (10:1). The organic layer was dried over Na2SO4, filtered and concentrated to yield a white solid of 5-(1,1,1-trifluoro-2-methylpropan-2-yl)isoxazol-3-amine (2 g, 9.06 mmol, 40.6% yield): 1H NMR (400 MHz, CDCl3) δ 5.78 (s, 1H), 3.93 (s., 2H), 1.51 (s, 6H); ES-LCMS m/z 195 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09035063B2
Source datasetuspto-grants-2015_05
ORD IDord-e79275bd8ec04d0bbc00b51fd77da920
Source noteuspto-grants-2015_05