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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102878Generated: October 25, 2026

Mesoxalic acid → 8-Benzyl-8-azabicyclo(3.2.1)octan-3-one

https://huagongshe.com/reaction/2102878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMesoxalic acidHCID 10132—
ReactantSodium HydroxideHCID 14798—
Reactant2,5-DimethoxytetrahydrofuranHCID 79098—
ReactantSodium AcetateHCID 517045—
ReactantBenzylammonium chlorideHCID 2724127—
SolventHydrochloric AcidHCID 313—
Product8-Benzyl-8-azabicyclo(3.2.1)octan-3-oneHCID 119846—

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 2,5-dimethoxytetrahydrofuran (50 g, 378 mmol) in 0.025M aqueous hydrochloric acid (160 ml) was cooled to 0° C. and stirred for 16 hours. Benzylamine hydrochloride (65 g, 453 mmol), ketomalonic acid (55 g, 377 mmol) and an aqueous solution of sodium acetate (300 ml, 0.69M) were added and the reaction stirred at room temperature for 1 hour. The mixture was heated to 50° C. for a further 90 minutes then cooled in an ice bath and basified to pH12 with 2N aqueous sodium hydroxide solution. The layers were separated, and the aqueous phase extracted with ethyl acetate (3×). The combined organic solutions were washed with water, dried (MgSO4), filtered and evaporated under reduced pressure. The residual brown oil was distilled under reduced pressure (126° C./0.4 kPa) to afford the title compound as an off-white solid, 37.81 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576097B2
Source datasetuspto-grants-2009_08
ORD IDord-839b530db7b544929b83f0f6e2767524
Source noteuspto-grants-2009_08