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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1580131Generated: November 1, 2026

Ethanol → HCID 68145452, compound

https://huagongshe.com/reaction/1580131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 12286596HCID 12286596—
SolventBenzeneHCID 241—
ProductHCID 68145452HCID 6814545294.2%

Reaction Steps

A mixture of 21.73 g of 1-(3-methoxyphenyl)-6-azabicyclo[3,2,1]octane-4,7-dione, 4.9 g of hydrazine hydrate and 170 ml of ethanol is refluxed for 1 hour. After cooling, the mixture is evaporated under reduced pressure to remove solvent. The residue thus obtained is dispersed in benzene and then filtered to give 21.64 g of 1-(3-methoxyphenyl)-6-azabicyclo[3,2,1]octane-4,7-dione-4-hydrazone as crude crystals. A mixture of 21.64 g of 1-(3-methoxyphenyl)-6-azabicyclo[3,2,1]octane-4,7-dione-4-hydrazone, 17.1 g of potassium tert.-butoxide and 400 ml of toluene is refluxed for 2 hours under heating. After cooling, water is added to the mixture, and the aqueous mixture is extracted with ether. The ether extract is washed with water, dried and then evaporated to remove solvent. The residue thus obtained is recrystallized from a mixture of ethylacetate and n-hexane. 17.54 g of 1-(3-methoxyphenyl)-6-azabicyclo[3,2,1]octane-7-one are obtained. M.p. 109° - 111°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03932429
Source datasetuspto-grants-1976_01
ORD IDord-d5b978bdb5e54dec90fbc83440b54dc4
Source noteuspto-grants-1976_01