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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904801Generated: October 31, 2026

HCID 20038045, compound → HCID 20038049, compound

https://huagongshe.com/reaction/1904801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 20038045HCID 20038045—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 20038049HCID 20038049—

Reaction Steps

Following the procedure of Example 3, a solution of 6.0 g of 3-n-decyl-1-(4-nitrophenyl)-3-azabicyclo[3.1.0]hexane-2,4-dione in 120 ml of ethanol is hydrogenated in the presence of 0.3 g of 5% palladium on carbon and worked up, affording the title compound which melts at 92°-94° C. after recrystallisation from ethyl acetate. The starting material is synthesised in accordance with Example 3, starting from 4.6 g of 1-(4-nitrophenyl)-3-azabicyclo[3.1.0]hexane-2,4-dione, 0.72 g of sodium hydride (pract. Fluka) and 5.3 ml of 1-decyl bromide. The product is a yellow oil with Rf=0.50 on thin-layer silica gel plates in the system hexane/ethyl acetate (1:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04839379
Source datasetuspto-grants-1989_06
ORD IDord-593951b8c9a44b80b6c8eb60c9c10299
Source noteuspto-grants-1989_06