Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2064958Generated: November 2, 2026

Hydrochloric Acid → 1-[5-(4-Nitro-pyrazol-1-ylmethyl)-isoxazol-3-yl]-ethanol

https://huagongshe.com/reaction/2064958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantNitrogenHCID 947—
ReactantAmmonium ChlorideHCID 25517—
ReactantTrimethylaluminumHCID 16682925—
ReactantHCID 86650887HCID 86650887—
SolventDichloromethaneHCID 6344—
SolventHeptaneHCID 8900—
Product1-[5-(4-Nitro-pyrazol-1-ylmethyl)-isoxazol-3-yl]-ethanolHCID 66928875—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 5-(4-nitro-pyrazol-1-ylmethyl)-isoxazole-3-carbaldehyde (666 mg, 3.00 mmol) in CH2Cl2 (22.0 mL) was treated at 0° C. with trimethylaluminum (15 mL of a 1M solution in heptane, 15.00 mmol). The reaction mixture was then stirred at 0° C. for 2 h. CH2Cl2 (100.0 mL) followed by sat. aq. NH4Cl (50 mL) was then added. The mixture was then treated with 1N HCl and the aq. layer was extracted with CH2Cl2 (20 mL). The combined org. extracts were dried over MgSO4, filtered, and the solvents were removed under reduced pressure to give the title compound as a green oil. LC-MS-conditions 02: tR=0.72 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288419B2
Source datasetuspto-grants-2012_10
ORD IDord-de56d9487d734e7199e653dbf3038f46
Source noteuspto-grants-2012_10