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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379571Generated: October 31, 2026

Hydrochloric Acid → HCID 18957477, compound

https://huagongshe.com/reaction/2379571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-Bromo-2-(cyclopentyloxy)-1-methoxybenzeneHCID 9970392—
Reactant3-(1-Methylethoxy)-2-cyclopenten-1-oneHCID 18957480—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18957477HCID 18957477—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 4-bromo-2-cyclopentyloxy-1-methoxybenzene (preparation 4) (9.50 g, 35.0 mmol) in tetrahydrofuran (70 ml) at -78° C. under an argon atmosphere was added dropwise n-butyllithium (15 ml of 2.5M solution, 37.5 mmol). The resulting mixture was stirred at -78° C. for 1.25 hr and added dropwise to a cooled solution (0° C.) of 3-isopropoxy-2-cyclopentenone (4.95 g, 35.3 mmol) in tetrahydrofuran (20 ml). Upon completion of the addition, the reaction mixture was allowed to warm to room temperature and was stirred for 1.5 hr. Hydrochloric acid (70 ml of 0.6N solution) was added to the reaction mixture and stirring was continued for 2.5 hr. The reaction mixture was poured into water and extracted with methylene chloride (four times). The combined organic extracts were dried (magnesium sulfate), the solvent was removed in vacuo and the residue was purified by flash chromatography, eluting with 1:4:5 methylene chloride/ether/hexanes. Recrystallization from methylene chloride/ether/hexanes provided needles (5.5 g, 63%): m.p. 136°-137° C. Analysis:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05362915
Source datasetuspto-grants-1994_11
ORD IDord-4ef10986ae2e44919ff74965a1a27c62
Source noteuspto-grants-1994_11