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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049003Generated: October 27, 2026

3-(4-Fluorobenzoyl)propyl chloride → 1-Phenyl-3-azabicyclo[3.1.0]hexane hydrochloride

https://huagongshe.com/reaction/2049003

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(4-Fluorobenzoyl)propyl chlorideHCID 19750—
Reactant1-Phenyl-3-azabicyclo[3.1.0]hexaneHCID 10130094—
CatalystPotassium IodideHCID 4875—
SolventTolueneHCID 1140—
Product1-Phenyl-3-azabicyclo[3.1.0]hexane hydrochlorideHCID 1271984359.4%

Reaction Steps

A mixture of 15.9 g of 1-phenyl-3-azabicyclo[3.1.0]hexane (Example 9), 20.1 g of γ-chloro-p-fluorobutyrophenone and 10 mg of potassium iodide in 100 ml of toluene is refluxed for 24 hours. Filtration gives 11.6 g of 1-phenyl-3-azabicyclo[3.1.0]hexane hydrochloride, m.p. 166°-167° C. Evaporation of the filtrate gives a brown oil which is combined with 2 N hydrochloric acid and chloroform. The crystals which form in the chloroform layer are collected by filtration and recrystallized from ethanol to give 3.10 g of 3-[3-(p-flurorbenzoyl)propyl]-1-phenyl-3-azabicyclo[3.1.0]hexane hydrochloride as pale tan crystals, m.p. 151°-153° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04196120
Source datasetuspto-grants-1980_04
ORD IDord-3251557012594aabb1298878b73de4da
Source noteuspto-grants-1980_04