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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1580132Generated: October 31, 2026

Toluene → HCID 12286599, compound

https://huagongshe.com/reaction/1580132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 68145452HCID 68145452—
SolventWaterHCID 962—
ProductHCID 12286599HCID 1228659990.9%

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-359e53422df1401f88dfa54ef5ee5b1f
Source noteuspto-grants-1976_01