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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 128747Erstellt: 25. Oktober 2026

Tetrahydrofuran → trans-2-(4-Hydroxycyclohexyl)-isoindole-1,3-dione

https://huagongshe.com/reaction/128747

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktN-CarbethoxyphthalimideHCID 31187—
EduktSodium BicarbonateHCID 516892—
Edukt(1s,4s)-4-Aminocyclohexan-1-ol hydrochlorideHCID 522619—
LösungsmittelWaterHCID 962—
Produkttrans-2-(4-Hydroxycyclohexyl)-isoindole-1,3-dioneHCID 28872672,4%

Reaktionsschritte

A solution of 4-aminocyclohexanol hydrochloride (6.08 g, 0.04 mole) in water (60 ml) was brought to pH 8 with aqueous sodium bicarbonate solution. N-carbethoxy-phthalimide (8.76 g, 0.04 mole) was added followed by tetrahydrofuran (until homogenous solution was obtained). The clear solution was stirred at room temperature overnight. During this time a white solid was precipitated. The tetrahydrofuran was removed in vacuo and the remaining aqueous solution was extracted with ethyl acetate until the solution was clear. The ethyl acetate extracts were combined, washed with water, dried (MgSO4) and concentrated to give 4-phthalimido cyclohexanol as a white solid (7.1 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05464864
Quelldatensatzuspto-grants-1995_11
ORD IDord-8ec7e128fb84498fa001bb7b74ba420b
Quellennotizuspto-grants-1995_11