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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Mesoxalic acid | HCID 10132 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,5-Dimethoxytetrahydrofuran | HCID 79098 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Benzylammonium chloride | HCID 2724127 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 8-Benzyl-8-azabicyclo(3.2.1)octan-3-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06586430B1 |
|---|
| Source dataset | uspto-grants-2003_07 |
|---|
| ORD ID | ord-4af99d93c7634c4481c5ef40602cf271 |
|---|
| Source note | uspto-grants-2003_07 |
|---|