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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371949Generated: October 26, 2026

3-Acetyl-1-(p-aminophenyl)-3-azabicyclo[3.1.0]hexane → 3-Acetyl-1-(p-hydroxyphenyl)-3-azabicyclo[3.1.0]hexane

https://huagongshe.com/reaction/371949

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Acetyl-1-(p-aminophenyl)-3-azabicyclo[3.1.0]hexaneHCID 20468332—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
Product3-Acetyl-1-(p-hydroxyphenyl)-3-azabicyclo[3.1.0]hexaneHCID 20352243—

Reaction Steps

A solution of 3-acetyl-1-(p-aminophenyl)-3-azabicyclo[3.1.0]hexane in 8N hydrochloric acid is diazotized at 0° C, with aqueous sodium nitrite. The solution is then allowed to stand at ambient temperature until the evolution of nitrogen ceases. This mixture is then extracted with ether, and the extract is dried over sodium sulfate, filtered and then evaporated under reduced pressure to give 3-acetyl-1-(p-hydroxyphenyl)-3-azabicyclo[3.1.0]hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04088652
Source datasetuspto-grants-1978_05
ORD IDord-70693089ac8046d4a43e434b407e55c4
Source noteuspto-grants-1978_05