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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992043Generated: October 31, 2026

Hydrochloric Acid → 8-Benzyl-8-azabicyclo(3.2.1)octan-3-one

https://huagongshe.com/reaction/1992043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzylamineHCID 7504—
ReactantSodium HydroxideHCID 14798—
ReactantAcetonedicarboxylic acidHCID 68328—
Reactant2,5-DimethoxytetrahydrofuranHCID 79098—
ReactantSodium AcetateHCID 517045—
SolventWaterHCID 962—
Product8-Benzyl-8-azabicyclo(3.2.1)octan-3-oneHCID 119846—

Reaction Conditions

Temperature0 °C

Reaction Steps

To cooled 192 ml of 0.025M HCl at 0° C. was added 60 g (454 mmol) of 2,5-dimethoxytetrahydrofuran and the mixture was stirred at 0° C. for 17 hrs. Then sequentially 78 g (543.6 mmol) of benzyl amine, 66 g (452.0 mmol) of 3-oxopentanedioic acid, and 20.4 g (248.4 mmol) of sodium acetate in 360 ml of water was added all at 0° C. The mixture was allowed to warm to room temperature and was stirred at room temperature for 1 hr. The mixture was clear, golden yellow in color. The mixture was heated to 50° C. for 2 hrs. The mixture turned cloudy. The mixture was then cooled to ambient temperature and adjusted to pH˜12 using 50% NaOH in water. The mixture was extracted with ethyl acetate (×3), dried over sodium sulfate and removed solvent to yield a brown oil. The mixture was further purified by distillation, desired product collected ˜120° C. 25 g crude product was recovered as a yellow oil to be carried on to next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07645771B2
Source datasetuspto-grants-2010_01
ORD IDord-9b17fdfd5ba5447a8e529358d79324ae
Source noteuspto-grants-2010_01