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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370409Generated: October 30, 2026

Hydrochloric Acid → HCID 86670681, compound

https://huagongshe.com/reaction/2370409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiiodomethaneHCID 6346—
Reactant1,2-DiiodoethaneHCID 12224—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 67256161HCID 67256161—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86670681HCID 86670681—

Reaction Steps

Under nitrogen flow, anhydrous THF (1 ml) was combined with Sm (705 mg, 4.7 mmol), and a solution of 1,2-diiodoethane (662 mg, 2.3 mmol) dissolved in anhydrous THF (2 ml) was added dropwise with stirring. The reaction solution was stirred for 30 minutes at room temperature. Thereafter, while cooling with ice, a solution of diiodomethane (723 mg, 2.7 mmol) and 5-(4-chlorobenzyl)-2-trifluoromethylcyclopentanone (Compound (V), (Ra)Xana=H, (Rb)Xbnb=CF3, Ym=4-Cl) (432 mg, 1.6 mmol) dissolved in anhydrous THF (2 ml) was added dropwise, and stirring was continued for 2 hours at room temperature. The reaction solution was poured into a solution mixture of an aqueous solution of NaOH (NaOH (1.1 g) dissolved in 10 ml of water) and THF (10 ml), and stirring was continued for 30 minutes at room temperature. This reaction solution was combined with ice, neutralized with a 1N aqueous solution of hydrochloric acid, and then extracted with hexane. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was distilled away under reduced pressure. Silica gel chromatography (eluent; hexane: ethyl acetate=70:1) was conducted for purification to obtain the desired substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710090B2
Source datasetuspto-grants-2014_04
ORD IDord-cb3a6edf3a684951baee4718f6295e5b
Source noteuspto-grants-2014_04