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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 389442Erstellt: 24. Oktober 2026

Acetone → 4-(4-iodo-1H-pyrazol-1-yl)cyclohexanone

https://huagongshe.com/de/reaction/389442

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetoneHCID 180—
EduktBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
Edukt1-(1,4-Dioxaspiro[4.5]dec-8-yl)-4-iodo-1H-pyrazoleHCID 59541125—
LösungsmittelWaterHCID 962—
Produkt4-(4-iodo-1H-pyrazol-1-yl)cyclohexanoneHCID 5954116594,1%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A mixture of 1-(1,4-dioxa-spiro[4.5]dec-8-yl)-4-iodo-1H-pyrazole (338 mg, 1.00 mmol), pyridinium p-toluenesulfonate (518 mg, 2.00 mmol), acetone (15 mL) and H2O (15 mL) was heated at 60° C. for 2 d. The mixture was extracted with EtOAc (3×30 mL). The combined extracts were washed with water (3×30 mL), brine (30 mL), dried over MgSO4, and concentrated in vacuo leaving 273 mg (89%) of the title compound as a white solid. 1H NMR (400 MHz, CDCl3): δ 2.23-2.63 (m, 8 H), 4.57-4.64 (m, 1 H), 7.51 (s, 1 H), 7.54 (s, 1 H). MS (ESI): 291.09 [M+H]+; HPLC tR=2.80 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08378104B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-dadb140749e848dcafc4fa6e18ef3b03
Quellennotizuspto-grants-2013_02