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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771389Generated: November 2, 2026

Hydrochloric Acid → HCID 86711510, compound

https://huagongshe.com/reaction/1771389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant4-Methoxyphenylhydrazine hydrochlorideHCID 2723904—
Reactant3-oxo-3-(tetrahydrofuran-3-yl)propanenitrileHCID 54595601—
SolventEthanolHCID 702—
ProductHCID 86711510HCID 86711510—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 3-oxo-3-(tetrahydrofuran-3-yl)propanenitrile (718 mg, 4.64 mmol) in EtOH (20 mL) was added conc. hydrochloric acid (0.387 mL, 4.64 mmol) and (4-methoxyphenyl)hydrazine hydrochloride (737 mg, 4.22 mmol). The reaction mixture was heated to 80° C. for 4 hr and was then cooled to RT and adjusted to pH8 by the addition of aq NaOH (2M, <5 mL). The resulting mixture was partitioned between water (20 mL) and Et2O (25 mL) and the aq layer was separated and extracted with ether (25 mL). The combined organic extracts were dried and evaporated in vacuo and the residue was purified by flash column chromatography (SiO2, 40 g, 0-5% MeOH in DCM, gradient elution) to afford the title compound, Intermediate A12, as a pale orange solid (503 mg, 45%); Rt 1.04 min (Method 2); m/z 260 (M+H)+, (ES+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249125B2
Source datasetuspto-grants-2016_02
ORD IDord-202cc32f718249f98e7d92cd80a4791d
Source noteuspto-grants-2016_02