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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258243Generated: October 26, 2026

Morpholine → Morpholine, 4-tetradecyl-

https://huagongshe.com/reaction/258243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantMyristyl bromideHCID 8208—
SolventAcetonitrileHCID 6342—
ProductMorpholine, 4-tetradecyl-HCID 11761694%

Reaction Steps

In a 250-mL round bottom flask, equipped with a magnetic stirrer, a heating mantle and reflux condenser, were placed 1-bromotetradecane (15.9 g, 57.3 mmol), acetonitrile (75 mL), and morpholine (10 g, 114.7 mmol). The reaction mixture was refluxed for 4 hrs. The reaction mixture was cooled to room temperature and was concentrated to a residue on a rotary evaporator. Water and ethyl acetate were added. The organic phase was separated and washed with saturated sodium chloride solution, and then dried over anhydrous magnesium sulfate. After filtration, the solvent was evaporated to dryness affording 15.2 g (94% yield) of 4-tetradecylmorpholine as a tan oil. This intermediate was subjected to the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05266567
Source datasetuspto-grants-1993_11
ORD IDord-4915d56f036b428187c79fe574ec5742
Source noteuspto-grants-1993_11