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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1653685Generated: October 26, 2026

Benzyl chloroformate → N-(Benzyloxycarbonyl)-5-fluorotryptamine

https://huagongshe.com/reaction/1653685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
Reactant5-FluorotryptamineHCID 164682—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductN-(Benzyloxycarbonyl)-5-fluorotryptamineHCID 994866568%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a strirred solution of 0.83 g (4-6 mmol) of 5-fluorotryptamine and 0.48 g (0.55 mL, 5 mmol) of nmethylmorpholine in 10 mL of DMF at 0° C. was added dropwise 0.72 mL (5 mmol) of benzylchloroformate. The reaction mixture was allowed to stir at 0° C. under argon. After 1.5 hours of stirring, the reaction mixture was 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 resulting residue was purified by flash chromatography using hexane:ethyl acetate (2:1) as an eluent to yield 1 g (68%) of N-(Benzyloxycarbonyl)-5-fluorotryptamine as a white solid. mp 104°-105° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05403851
Source datasetuspto-grants-1995_04
ORD IDord-c926f55aecc74952957baf79dd642aa0
Source noteuspto-grants-1995_04