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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1467918Erstellt: 26. Oktober 2026

Methyl Acrylate → 6'-Isobutoxyspiro[cyclohexane-1,2'-indene]-1',4(3'H)-dione

https://huagongshe.com/reaction/1467918

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl AcrylateHCID 7294—
EduktPotassium HydroxideHCID 14797—
EduktPotassium tert-butoxideHCID 23665647—
Edukt6'-bromo-4-methoxyspiro[cyclohexane-1,2'-inden]-1'(3'H)-oneHCID 58197263—
LösungsmittelWaterHCID 962—
LösungsmittelSodium chloride; waterHCID 57417360—
Produkt6'-Isobutoxyspiro[cyclohexane-1,2'-indene]-1',4(3'H)-dioneHCID 6797931956,3%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a mixture of 6-isobutoxy-2,3-dihydro-1H-inden-1-one (Intermediate 4, 17.4 g, 85 mmol) and methyl acrylate (16.9 mL, 187 mmol) in 2-Me THF (84 mL) cooled to 0° C. was added potassium tert-butoxide (11.8 g, 102 mmol) in portions over 3 min. After stirring at r.t. for 2.5 h more potassium tert-butoxide (2.95 g, 25.5 mmol) was added at 0° C. After stirring at r.t. for 2.5 h were water (126 mL) and potassium hydroxide (4.77 g, 85 mmol) added and the mixture was heated at reflux overnight. The mixture was allowed to cool to r.t. and brine was added. The layers were separated and the aqueous layer was re-extracted with EtOAc twice. The combined organic layers were dried over Na2SO4, filtered and evaporated to yield the title compound (13.7 g, 56% yield). 1H NMR (400 MHz, CDCl3) δ ppm 1.04 (m, 8 H) 1.86 (m, 2 H) 2.11 (dt, 1 H) 2.21 (m, 2 H) 2.47 (m, 3 H) 2.70 (m, 2 H) 3.15 (s, 2 H) 3.76 (m, 3 H) 7.20 (m, 1 H) 7.25 (m, 1 H) 7.38 (d, 1 H); MS (ES+) m/z 287 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09000182B2
Quelldatensatzuspto-grants-2015_04
ORD IDord-a86c3bc729b4494fb698878e16cc1a46
Quellennotizuspto-grants-2015_04