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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1749711Erstellt: 26. Oktober 2026

Formaldehyde → Tert-butyl 4-[(5-chloro-6-hydroxy-3-oxo-2,3-dihydrobenzofuran-7-yl)methyl]piperazine-1-carboxylate

https://huagongshe.com/reaction/1749711

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
Edukt5-chloro-6-hydroxybenzofuran-3(2H)-oneHCID 57443549—
LösungsmittelEthanolHCID 702—
ProduktTert-butyl 4-[(5-chloro-6-hydroxy-3-oxo-2,3-dihydrobenzofuran-7-yl)methyl]piperazine-1-carboxylateHCID 7127850656,4%

Reaktionsschritte

A solution of 5-chloro-6-hydroxybenzofuran-3(2H)-one (0.185 g, 1.00 mmol) in ethanol (20 mL) was added with 1-tert-butoxycarbonylpiperazine (0.186 g, 1.00 mmol), and 37% aqueous formaldehyde (0.0812 g, 1.00 mmol) at room temperature. The mixture was stirred overnight at room temperature, and then the precipitates formed were collected by filtration, and then washed with ethyl acetate to obtain tert-butyl 4-[(5-chloro-6-hydroxy-3-oxo-2,3-dihydrobenzofuran-7-yl)methyl]piperazine-1-carboxylate (0.216 g, 56%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09156827B2
Quelldatensatzuspto-grants-2015_10
ORD IDord-7fbf3da338ed494fbb552cb3a247000b
Quellennotizuspto-grants-2015_10