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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079375Generated: October 30, 2026

Triethylamine → N-(p-methoxybenzyloxycarbonyl)-5-fluorotryptamine

https://huagongshe.com/reaction/1079375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,4-DioxaneHCID 31275—
Reactant5-FluorotryptamineHCID 164682—
Reactant2-(4-Methoxybenzyloxycarbonyloxyimino)-2-phenylacetonitrileHCID 3916227—
SolventWaterHCID 962—
ProductN-(p-methoxybenzyloxycarbonyl)-5-fluorotryptamineHCID 1537989163.7%

Reaction Steps

To a strirred suspension 1.4 g (7.8 mmol) of 5-fluorotryptamine in 5 mL of water and 1.1 mL (7.8 mmol) of triethylamine was added 2.5 g (7.8 mmol) of 2-(4-methoxybenzyloxycarbonyloxyimino)-2-phenylacetonitrile (MOZ-ON) and 10 mL of dioxane. The reaction mixture was stirred at room temperature for 1 hour under argon, diluted with water, and extracted with ethyl acetate. The organic extracts were washed with saturated sodium chloride, dried over anhydrous Na2SO4, and concentrated under vacuum. The residue was purified by flash chromatography, over silica gel, using hexane:ethyl acetate (2:1 and later 1:1) as eluents to provide 1.7 g (63%) of N-(p-methoxybenzyloxycarbonyl)-5-fluorotryptamine as an off-white solid. mp 118°-119° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05580878
Source datasetuspto-grants-1996_12
ORD IDord-33d87a995c4a45d68ccf3f9f191d7c87
Source noteuspto-grants-1996_12