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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 237765Generated: October 30, 2026

Hydrochloric Acid → HCID 68524570, compound

https://huagongshe.com/reaction/237765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCyclohexanoneHCID 7967—
Reactant2-Bromo-5-hydroxypyridineHCID 2762865—
ReactantButyllithiumHCID 178418339—
ReactantCID 53628100HCID 178418400—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68524570HCID 6852457047.4%

Reaction Steps

To a solution of 6-bromo-pyridin-3-ol (5.0 g, 28.7 mmol) in anhydrous THF (75 mL) and anhydrous toluene (40 mL) at −78° C. was added n-butyllithium (2.5 M in hexane, 28.73 mmol). The mixture was stirred for 20 min. A solution of sec-butyllithium (1.4 M in cyclohexane, 43.1 mmol) was added dropwise and the mixture stirred at −78° C. for 1 hour. To the mixture was added cyclohexanone (4.23 g, 43.1 mmol) in THF (25 mL) at −78° C. and the mixture stirred at −78° C. for 1 hour. Saturated NaH2PO4 solution (10 mL) was slowly added to the mixture and the mixture then warmed to room temperature. Water (300 mL) was added. The reaction mixture was neutralized with hydrochloric acid (2N), and the mixture extracted three times with EtOAc. The organic layer was washed with brine and dried (Na2SO4). Silica gel chromatography (EtOAc/heptane) provided 2.63 g of the title compound. C11H15NO2 (193.11), LCMS (ESI): 194.09 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642603B2
Source datasetuspto-grants-2014_02
ORD IDord-86efa231545948d5a42a96a767f81146
Source noteuspto-grants-2014_02