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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355370Generated: October 25, 2026

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

https://huagongshe.com/reaction/1355370

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 Steps

A solution of 2,5 dimethoxytetrahydrofuran (50 g, 378 mmol) in 0.025M hydrochloric acid (160 ml) was cooled to 0° C. 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 and then cooled in an ice bath whilst basifying to pH12 with 2N 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. @ 3 mm of Hg) to afford the title compound as an off-white solid, 37.81 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586430B1
Source datasetuspto-grants-2003_07
ORD IDord-4af99d93c7634c4481c5ef40602cf271
Source noteuspto-grants-2003_07