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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366188Generated: November 2, 2026

Iodine → HCID 57589953, compound

https://huagongshe.com/reaction/1366188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantNitrogenHCID 947—
ReactantSodium borohydrideHCID 4311764—
Reactant2,2,2-Trifluoro-1-[4-(4-nitrophenyl)piperidin-1-yl]ethan-1-oneHCID 54285760—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57589953HCID 57589953—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 1-trifluoroacetyl-4-(4-nitrophenyl)piperidine (1.42 g, 4.7 mmol) in THF (15 mL) is stirred in 25 mL 2-necked flask fitted with a condenser and pressure-equalising addition funnel. The system is flushed with N2, NaBH4 (210 mg, 5.6 mmol) is added and the flask is cooled to 0° C. A solution of iodine (600 mg, 2.3 mmol) in THF (5 mL) is then added dropwise over 20 minutes, after which the addition funnel is removed and the mixture heated at reflux overnight. The resulting pale yellow suspension is cooled to rt and MeOH (1.5 mL) is added cautiously, causing vigorous evolution of a gas. Evaporation of the solvents affords the title compound, which is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893058B2
Source datasetuspto-grants-2011_02
ORD IDord-be65ed07ae6a436ba8f8ade2db91e952
Source noteuspto-grants-2011_02