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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3332Generated: November 3, 2026

Hydrochloric Acid → HCID 18934737, compound

https://huagongshe.com/reaction/3332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyrrolizinium, 1,2,3,5,6,7-hexahydro-, perchlorateHCID 10878400—
Reactant3-Bromo-3-phenylpyridineHCID 18934767—
ReactantHCID 178418306HCID 178418306—
SolventDiethyl EtherHCID 3283—
SolventPentaneHCID 8003—
ProductHCID 18934737HCID 1893473714.5%

Reaction Conditions

Temperature-30 °C

Reaction Steps

3-Bromo-3-phenylpyridine (200 mg, 0.85 mmol) was dissolved in Et2O and cooled to -30° C. A solution of 2.5M t-BuLi (1.1 mL, 1.90 mmol) in pentane was added, and the reaction was stirred for 10 minutes. 1,2,3,5,6,7-Hexahydropyrrolizinium perchlorate (230 mg, 1.30 mmol) was added, and the reaction mixture was allowed to stir for 30 minutes at -30° C. then allowed to warm to room temperature and stir for 1 hour. Then 2N HCl was added, the phases were separated, and the aqueous phase was basified with 15% NaOH and extracted with CH2Cl2 (2×). The organic phases were combined, dried (MgSO4) and concentrated, and the residue was chromatographed (silica gel; CHCl3 /MeOH, 95:5) to afford a clear oil (32.5 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05733912
Source datasetuspto-grants-1998_03
ORD IDord-5b22770333014a4da72ab520662759f7
Source noteuspto-grants-1998_03