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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707734Generated: October 27, 2026

Morpholine → Morpholine, 4-tetradecyl-

https://huagongshe.com/reaction/1707734

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 numberUS05354862
Source datasetuspto-grants-1994_10
ORD IDord-6e9b304c6ccb4b4ca1bc9fb593431ef2
Source noteuspto-grants-1994_10