HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(p-methoxybenzyloxycarbonyl)-5-fluorotryptamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 5-Fluorotryptamine | HCID 164682 | — |
| Reactant | 2-(4-Methoxybenzyloxycarbonyloxyimino)-2-phenylacetonitrile | HCID 3916227 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(p-methoxybenzyloxycarbonyl)-5-fluorotryptamine | HCID 15379891 | 63.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05580878 |
| Source dataset | uspto-grants-1996_12 |
| ORD ID | ord-33d87a995c4a45d68ccf3f9f191d7c87 |
| Source note | uspto-grants-1996_12 |