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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1653686Generated: November 1, 2026

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

https://huagongshe.com/reaction/1653686

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 numberUS05403851
Source datasetuspto-grants-1995_04
ORD IDord-5b46a9795cd7442eacc8a8f4d50165cb
Source noteuspto-grants-1995_04