Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583456Generated: October 26, 2026

1-Adamantan-1-yl-ethanone oxime → Rimantadine

https://huagongshe.com/reaction/1583456

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Adamantan-1-yl-ethanone oximeHCID 2802269—
CatalystPlatinumHCID 23939—
SolventAcetic AcidHCID 176—
ProductRimantadineHCID 507196%

Reaction Steps

Into a Parr hydrogenation flask were placed 8.0 g of 1-adamantyl methyl ketoxime, 200 ml of glacial acetic acid, and 2.8 g of 5% Pt/C. Hydrogenation was continued overnight at 39 psia (270 KPa) and at ambient temperature. The catalyst was removed by filtration and the acetic acid solution was concentrated to one-third of the original volume by vacuum distillation. Water, 200 ml, was added to this conc. acetic acid solution and it was made basic with sodium hydroxide to give a milky solution. The milky solution was extracted three times with 100 ml of methylene chloride. The combined methylene chloride layer was dried over magnesium sulfate which was removed by filtration. The methylene chloride solution was distilled under vacuum to give 7.1 g of clear liquid rimantadine free base (96% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04551552
Source datasetuspto-grants-1985_11
ORD IDord-a9d5bc16315e41e68865ec9e0421dc66
Source noteuspto-grants-1985_11