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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356801Generated: October 27, 2026

Hexane → trans-N-(6,6-Dimethyl-2-hepten-4-ynyl)-N-methyl-[3-(1-ethylvinyl)benzyl]amine

https://huagongshe.com/reaction/1356801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactanttrans-3'-[N-(6,6-Dimethyl-2-hepten-4-ynyl)-N-methylaminomethyl]propiophenoneHCID 18509386—
ReactantButyllithiumHCID 178418339—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventBenzeneHCID 241—
Producttrans-N-(6,6-Dimethyl-2-hepten-4-ynyl)-N-methyl-[3-(1-ethylvinyl)benzyl]amineHCID 1206988550.5%

Reaction Steps

Methyl triphenylphosphonium bromide (0.72 g; 2.01 mmol) was added to benzene (15 ml). While the mixture was stirred under nitrogen atmosphere at room temperature, n-butyl lithium in n-hexane (1.56 M: 1.3 ml; 2.03 mmol) was added dropwise. The mixture was stirred for 5 minutes, and Compound 23 (0.40 g; 1.34 mmol) in benzene (5 ml) was added dropwise thereto, followed by heating under reflux for 2 hours. The mixture was brought to room temperature, and poured into ice/water, followed by extraction with benzene (100 ml). The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=20:1), to thereby yield 0.20 g of the target compound as pale yellow oily matter (yield: 50.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586633B1
Source datasetuspto-grants-2003_07
ORD IDord-d8cdd86947bc40fd834e0e8ed3c01c59
Source noteuspto-grants-2003_07