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HRID 28833Erstellt: 23. Oktober 2026

Potassium Hydroxide → Tert-butyl 4-[2-(1-benzothien-2-yl)-1-hydroxyethyl]piperazine-1-carboxylate

https://huagongshe.com/de/reaction/28833

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
Edukt2-(2,2-Dibromo-vinyl)benzo[b]thiopheneHCID 86599047—
LösungsmittelOxolane--water (1/1)HCID 21881883—
ProduktTert-butyl 4-[2-(1-benzothien-2-yl)-1-hydroxyethyl]piperazine-1-carboxylateHCID 6885133865,3%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

A 50 mL round bottom flask was charged with 2-(2,2-dibromo-vinyl)-benzo[b]thiophene (1.0 g, 3.17 mmol), tert-butyl 1-piperazinecarboxylate (0.09 g, 4.76 mmol) and potassium hydroxide (0.71 g, 12.5 mmol). A solution of tetrahydrofuran:water (4:1) was added and the solution was heated to 70° C. for 18 hours. At the end of this time the solution was concentrated and the residue was diluted with a 2N aqueious solution of hydrochloric acid and extracted 3 times with ethyl acetate. The ethyl acetate was dried and concentrated and the residue subjected chromatography via Biotage (FLASH 40 M, silica, 60% ethyl acetate/hexane) to yield 0.75 g (65%) of tert-butyl 4-[2-(1-benzothien-2-yl)-1-hydroxyethyl]piperazine-1-carboxylate as an off white solid. MS (ES) m/z 305.1; HRMS: calcd for C19H26N2O3S, 362.1664; found (ESI, [M+H]+), 361.1569.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07419980B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-da0390fcdd33407c97fe574ed64366a4
Quellennotizuspto-grants-2008_09