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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472678Generated: October 31, 2026

Allyl bromide → HCID 86651613, compound

https://huagongshe.com/reaction/472678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 86651612HCID 86651612—
CatalystZincHCID 23994—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 86651613HCID 86651613—

Reaction Steps

To a suspension of (2R)-N-{(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethyl}-4-{[(1,1-dimethylethyl)sulfinyl]imino}-2-(4-fluoro-2-methylphenyl)-N-methyl-1-piperidinecarboxamide (Intermediate 1, 50 mg, 0.082 mmol) and Zinc powder (16.14 mg, 0.247 mmol, Aldrich) in THF (1.5 mL) was added at 25° C. allyl bromide (0.021 mL, 0.247 mmol, Aldrich) and the reaction mixture was stirred at this temperature for 16 hrs. Brine and EtOAc were added and the resulting mixture was filtrated over Celite® and the two phases were separated. The aqueous phase was extracted with EtOAc (3×) and the combined organic phases were dried over Na2SO4 and evaporated to dryness. The crude was purified by flash chromatography on silica with SP1 (Biotage) system (from 1:0 to 0:1 Cyclohexane/EtOAc; 25M Si cartridge) to give two different products:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633214B2
Source datasetuspto-grants-2014_01
ORD IDord-af86b54ad2d94da6881160092dedb56a
Source noteuspto-grants-2014_01