Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783953Generated: October 30, 2026

Iodine → HCID 57589953, compound

https://huagongshe.com/reaction/1783953

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-equalizing 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 numberUS07501411B2
Source datasetuspto-grants-2009_03
ORD IDord-458f93ff7bf64ce7b249c7fe30a69a34
Source noteuspto-grants-2009_03