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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860761Generated: November 2, 2026

Naphthalene → 3-Cyclohexyl-4-morpholinoethoxybenzaldehyde

https://huagongshe.com/reaction/1860761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNaphthaleneHCID 931—
ReactantDimethylformamideHCID 6228—
ReactantLithiumHCID 3028194—
Reactant3-Cyclohexyl-4-morpholinoethoxychlorobenzeneHCID 54220254—
SolventTetrahydrofuranHCID 8028—
Product3-Cyclohexyl-4-morpholinoethoxybenzaldehydeHCID 5422617438.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Naphthalene (3.48 g, 27.2 mmol) was added to a suspension of 30% lithium dispersion (3.2 g, 138 mmol, pre-washed with tetrahydrofuran) in tetrahydrofuran (80 ml). The suspension was stirred until a green color appeared (approximately 1 hour). The reaction was cooled to −78° C., and a solution of the 3-cyclohexyl-4-morpholinoethoxy-chlorobenzene (8 g, 24.7 mmol) in tetrahydrofuran (20 ml) was added. After 1 hour, the reaction was warmed to 0° C. and stirred for an additional hour. Dimethylformamide (9.6 ml, 123.5 mmol) was added, the reaction was stirred at 0° C. for one more hour and then warmed to room temperature and stirred for another hour. The reaction was quenched with methanol (30 ml), added to 1N hydrochloric acid (300 ml) and extracted with ethyl acetate (400 ml). The organic layer was washed with water (300 ml), saturated sodium bicarbonate solution (300 ml) and brine (300 ml), dried over magnesium sulfate and concentrated. Chromatography (silica, 40-60% ethyl acetate/hexanes) afforded 3 g (34%) of 3-cyclohexyl-4-morpholinoethoxybenzaldehyde as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531502B1
Source datasetuspto-grants-2003_03
ORD IDord-9e2adc4a36394b7790c3e1e5148927d4
Source noteuspto-grants-2003_03