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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561213Generated: October 29, 2026

Triethylamine → HCID 86620459, compound

https://huagongshe.com/reaction/561213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCyanogen BromideHCID 10476—
Reactant4-(2-Bromo-5-fluorophenoxy)piperidineHCID 57832757—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86620459HCID 86620459—

Reaction Steps

To a solution of 4-(2-bromo-5-fluorophenoxy)piperidine (2.0 g, 7.30 mmol) in THF (24.3 ml) was added cyanogen bromide (0.77 g, 7.30 mmol) followed by triethylamine (1.01 ml, 7.3 mmol) at 0° C. The mixture was warmed to rt and further stirred for 1 h. Solvent was evaporated and the residue was diluted with 1N HCl (20 mL). The aqueous layer was extracted with EtOAc (3×10 mL). The combined organic fractions were washed with water (20 mL) and dried over Na2SO4. The solvent was evaporated under reduced pressure to afford the title compound as a solid which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063224B2
Source datasetuspto-grants-2011_11
ORD IDord-681af696eefd4038a401d315f39a9be5
Source noteuspto-grants-2011_11