Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242212Generated: October 31, 2026

Hydrochloric Acid → HCID 136350243, compound

https://huagongshe.com/reaction/242212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
ReactantDimethyl SulfideHCID 1068—
ReactantBoron trifluorideHCID 6356—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 86668982HCID 86668982—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 136350243HCID 13635024334.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4-(3,5-dimethylisoxazol-4-yl)-3-(4-methoxyphenyl)-1-methyl-1H-pyrazole-5-carbaldehyde (9.1 mg, 0.029 mmol), hydroxylamine hydrochloride (54.9 mg, 0.79 mmol) and pyridine (69 μL, 0.85 mmol) in dry EtOH (1 mL) was heated at 100° C. for 3 minutes in the microwave. 1 mL 2 M HCl and 5 mL DCM were added and the phases were separated. The organic phase was filtered through a phase separator and concentrated to give a raw product, that was dissolved in DCM (0.5 mL). BF3.Me2S (1 M solution in DCM, 0.5 mL, 0.5 mmol) was added and the mixture was stirred at room temperature over night. Methanol was added to quenched the reaction and the mixture was purified on preparative HPLC to give E12 4-(3,5-dimethylisoxazol-4-yl)-3-(4-hydroxyphenyl)-1-methyl-1H-pyrazole-5-carbaldehyde oxime (3.0 mg, 0.01 mmol, 32%). Identification of the title compound by 1H-NMR showed that the oxime product was a single isomer, but did not confirm whether the (E) or (Z) oxime isomer had been obtained. ES/MS m/z: 313.22 (M+H), 311.21 (M−H); 1H NMR (acetone-d6, 500 MHz): 7.92 (s, 1H), 7.31 (m, 2H), 6.79 (m, 2H), 4.08 (s, 3H), 2.15 (s, 3H) and 1.86 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653112B2
Source datasetuspto-grants-2014_02
ORD IDord-cd90bed817414b509a7a2c8cef64c0d1
Source noteuspto-grants-2014_02