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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1826357Generated: November 2, 2026

Hydrochloric Acid → 6-(3-Chlorophenyl)-3-hexyl-6-methyl-3-azabicyclo[3.1.0]hexane

https://huagongshe.com/reaction/1826357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(3-Hexyl-6-methyl-3-azabicyclo[3.1.0]hex-6-yl)phenylamineHCID 22141322—
ReactantSodium NitriteHCID 23668193—
CatalystCuprous chlorideHCID 62652—
SolventWaterHCID 962—
Product6-(3-Chlorophenyl)-3-hexyl-6-methyl-3-azabicyclo[3.1.0]hexaneHCID 2214121239%

Reaction Steps

A solution of sodium nitrite (97 mg, 1.4 mmol) dissolved in water (2 ml) was added to 3-(3-hexyl-6-methyl-3-azabicyclo[3.1.0]hex-6-yl)phenylamine (Preparation 12, 0.17 g, 0.61 mmol) dissolved in aqueous hydrochloric acid (2.0 M, 2 ml) over a few minutes at 0° C. After 30 min at 0° C., the reaction mixture was added to copper (I) chloride (1.57 g, 15.8 mmol) in concentrated hydrochloric acid (4.0 ml). After stirring the reaction mixture at room temperature for 45 min, the reaction mixture was heated to 90° C. for 5 min. The reaction mixture was poured cautiously on to solid, pre-wetted sodium hydrogen carbonate and the product was extracted firstly with diethyl ether and then ethyl acetate. The combined organic extracts were dried (MgSO4) and then concentrated in vacuo. The crude residue was purified by chromatography on silica gel eluting with hexane:ethyl acetate (8:1) to give the product (69 mg, 39%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07049444B2
Source datasetuspto-grants-2006_05
ORD IDord-9e98f0cc32fb4b79af6643bf14ebb23a
Source noteuspto-grants-2006_05