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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 539348Erstellt: 24. Oktober 2026

Water → N-(5-Bromo-4'-methoxy-3H-spiro[benzofuran-2,1'-cyclohexane]-3-ylidene)-2-methylpropane-2-sulfinamide

https://huagongshe.com/de/reaction/539348

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktTert-ButanesulfinamideHCID 3382465—
Edukt(5-Bromo-2-fluorophenyl)(1-hydroxy-4-methoxycyclohexyl)methanoneHCID 67979505—
KatalysatorTitanium tetraethoxideHCID 76524—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelHCID 178479889HCID 178479889—
ProduktN-(5-Bromo-4'-methoxy-3H-spiro[benzofuran-2,1'-cyclohexane]-3-ylidene)-2-methylpropane-2-sulfinamideHCID 6797952065%

Reaktionsschritte

To a mixture of 5-bromo-4′-methoxy-3H-spiro[benzofuran-2,1′-cyclohexan]-3-one (Intermediate 12, 2.8 g, 9.00 mmol) and 2-methylpropane-2-sulfinamide (2.024 g, 16.20 mmol) in methyl THF (15 mL) was added titanium ethoxide (3.71 mL, 18.00 mmol) and the reaction was heated to reflux. After 21 h the reaction was allowed to cool to r.t. whereafter it was diluted with EtOAc (150 mL). Water (12 mL) was added dropwise over 10 min under vigorous stirring and then the mixture was left standing without stirring for 1.5 h. The solids were filtered off and the organics were evaporated. The crude product was purified by flash chromatography using a gradient of 0%-50% EtOAc in heptane, yielding 2.41 g of the title compound (65% yield): 1H NMR (500 MHz, CDCl3) δ ppm 1.33 (s, 9 H), 1.81 (m, 6 H), 2.12 (d, 2 H), 3.33 (m, 1 H), 3.42 (s, 3 H), 6.94 (d, 1 H), 7.59 (dd, 1 H), 8.53 (m, 1 H); MS (ES+) m/z 415 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08865911B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-8c27dd4fceca4ead89fb8c6b2efb2e63
Quellennotizuspto-grants-2014_10