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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611237Generated: October 25, 2026

1-(2,6,6-Trimethylcyclohex-3-en-1-yl)but-2-en-1-one → 3-[3-(3-{3-[1-Methyl-3-oxo-3-(2,6,6-trimethyl-cyclohex-3-enyl)-propylamino]-propylamino}-propylamino)-propylamino)-1-(2,6,6-trimethyl-cyclohex-3-enyl)-butan-1-one

https://huagongshe.com/reaction/1611237

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2,6,6-Trimethylcyclohex-3-en-1-yl)but-2-en-1-oneHCID 42296—
ReactantNorspermineHCID 78350—
SolventEthanolHCID 702—
Product3-[3-(3-{3-[1-Methyl-3-oxo-3-(2,6,6-trimethyl-cyclohex-3-enyl)-propylamino]-propylamino}-propylamino)-propylamino)-1-(2,6,6-trimethyl-cyclohex-3-enyl)-butan-1-oneHCID 23591368—

Reaction Steps

To a 0° C. stirred solution of 96 g (0.50 mol) of 1-(2,6,6-trimethyl-cyclohex-3-enyl)-but-2-en-1-one (δ-damascone) in 250 mL of ethanol is added 47 g (0.25 mol) of N1-[3-(3-Amino-propylamino)-propyl]-propane-1,3-diamine. The reaction is allowed to warm to room temperature. After stirring for 24 h, the ethanol is concentrated by rotary evaporation to give 3-[3-(3-{3-[1-methyl-3-oxo-3-(2,6,6-trimethyl-cyclohex-3-enyl)-propylamino]-propylamino}-propylamino)-propylamino]-1-(2,6,6-trimethyl-cyclohex-3-enyl)-butan-1-one (bis-Michael adduct 14) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06987084B2
Source datasetuspto-grants-2006_01
ORD IDord-fd41c0a78b3e475e926c4ea332614834
Source noteuspto-grants-2006_01