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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816316Generated: November 4, 2026

Hydrochloric Acid → HCID 22985555, compound

https://huagongshe.com/reaction/1816316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantDichloromethane ethylacetateHCID 21226138—
ReactantHCID 22493572HCID 22493572—
SolventEthanolHCID 702—
ProductHCID 22985555HCID 22985555—

Reaction Conditions

Temperature100 °C

Reaction Steps

To 5 ml of 130 mg of α-(1-tert-butyl-5-isopropylpyrazol-3-yl)-4-(4,4-dimethyl-1,3-oxazolin-2-yl)styrene in ethanol was added 0.4 ml of a 3N aqueous solution of an acid at room temperature. The resulting mixture was heated under reflux for 30 minutes. To the reaction mixture was added a 5N aqueous solution of sodium hydroxide to adjust its pH to 11, followed by extraction with dichloromethane. The organic layer was washed with saturated saline, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. To a solution of the residue in 3 ml of 1,4-dioxane were added 100 mg of lithium hydroxide and the resulting mixture was heated at 100° C. for 2 hours. After the completion of the reaction, a 3N aqueous solution of hydrochloric acid was added to adjust the pH to 5, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue so obtained was subjected to chromatography on a silica gel column (developing solvent: 50% dichloromethane/ethyl acetate), whereby 4 mg of the title compound were obtained as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06884808B2
Source datasetuspto-grants-2005_04
ORD IDord-ba911d899c5243a38e95d71d8e23923d
Source noteuspto-grants-2005_04