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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536970Generated: October 26, 2026

Water → 4-(4-Amino-phenyl)-1,1-dioxo-hexahydro-1lambda6-thiopyran-4-carbonitrile

https://huagongshe.com/reaction/536970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-(4-Nitro-phenyl)-1,1-dioxo-hexahydro-1lambda6-thiopyran-4-carbonitrileHCID 58994932—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
Product4-(4-Amino-phenyl)-1,1-dioxo-hexahydro-1lambda6-thiopyran-4-carbonitrileHCID 5899503462%

Reaction Conditions

Temperature50 °C

Reaction Steps

A suspension of 4-(4-nitro-phenyl)-1,1-dioxo-hexahydro-1λ6-thiopyran-4-carbonitrile (205 mg, 0.731 mmol, as prepared in the previous step) in EtOH (5 mL) and water (5 mL) was treated with solid NH4Cl (204 mg, 3.66 mmol) and Fe powder (392 mg, 7.31 mmol) and heated to 50° C. for 1.5 h. The cooled mixture was filtered through Celite, and the filter cake was washed with MeOH. The solvents were evaporated in vacuo. The residue was diluted with water (30 mL) and extracted with EtOAc (2×30 mL). The combined organic layers were dried over MgSO4 and concentrated in vacuo. Silica gel chromatography of the residue on a 50-g Varian MegaBond Elut SPE column with 50% EtOAc-hexane afforded the title compound (114 mg, 62%) as a pale yellow solid. Mass spectrum (ESI, m/z): Calcd. for C12H14N2O2S, 251.1 (M+H). found 251.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859602B2
Source datasetuspto-grants-2014_10
ORD IDord-cb951d0b0bff4ac2b6c5721c867feab1
Source noteuspto-grants-2014_10