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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1407534Erstellt: 26. Oktober 2026

3-Bromophenol → 3-(4,5-difluoro-2-hydroxyphenyl)-1-(diphenylmethyl)-3-hydroxy-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/reaction/1407534

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-BromophenolHCID 11563—
Edukt3,4-DifluorophenolHCID 75927—
Edukt1-(diphenylmethyl)-1H-indole-2,3-dioneHCID 1969277—
Edukt1-((5-(Trifluoromethyl)furan-2-yl)methyl)indoline-2,3-dioneHCID 67356488—
Produkt3-(4,5-difluoro-2-hydroxyphenyl)-1-(diphenylmethyl)-3-hydroxy-1,3-dihydro-2H-indol-2-oneHCID 67357429—

Reaktionsschritte

Following the procedure as described in PREPARATION 2A and making non-critical variations using 3,4-difluorophenol to replace 3-bromophenol, and 1-(diphenylmethyl)-1H-indole-2,3-dione to replace 1-((5-(trifluoromethyl)furan-2-yl)methyl)indoline-2,3-dione, 3-(4,5-difluoro-2-hydroxyphenyl)-1-(diphenylmethyl)-3-hydroxy-1,3-dihydro-2H-indol-2-one was obtained (61%) as a colorless solid: 1H NMR (300 MHz, CDCl3) δ9.23 (br s, 1H), 7.47-7.44 (m, 1H), 7.35-7.21 (m, 9H), 7.18-7.11 (m, 2H), 6.90 (s, 1H), 6.83 (dd, J=11.2, 6.9 Hz, 1H), 6.67 (dd, J=11.2, 8.7 Hz, 1H), 6.56-6.51 (m, 1H), 4.13 (br s, 1H); MS (ES+) m/z 426.2 (M−17).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08916580B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-89147ad5c2a147cd9d9ef240cfb534a0
Quellennotizuspto-grants-2014_12