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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2201628Erstellt: 25. Oktober 2026

Thiophenol → 8-fluoro-6-phenylsulfanyl-3,4-dihydro-2H-naphthalen-1-one

https://huagongshe.com/reaction/2201628

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThiophenolHCID 7969—
EduktTriethylamineHCID 8471—
EduktHeptaneHCID 8900—
Edukt6,8-Difluoro-3,4-dihydronaphthalen-1(2H)-oneHCID 55274581—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylacetamideHCID 31374—
Produkt8-fluoro-6-phenylsulfanyl-3,4-dihydro-2H-naphthalen-1-oneHCID 5902176979%

Reaktionsschritte

A solution of 6,8-difluoro-3,4-dihydro-2H-naphthalen-1-one (1.58 kg) in N,N-dimethylacetamide (4.65 liters) was treated with triethylamine (877 g) and thiophenol (954.9 g) at 20° C. and the reaction mixture was stirred for 19 hours. The reaction mixture was treated with heptane (2.38 liters.), followed by water (9.5 liters) and the precipitate was isolated by filtration and the resulting slurry washed with twice with heptane (790 ml each time), three times with water (1.0 liters each time) and five times with cyclohexane (1.0 liters, each time). The slurry was dried to give 8-fluoro-6-phenylsulfanyl-3,4-dihydro-2H-naphthalen-1-one (1.86 kg, 79% yield) with a purity of 96.2% by HPLC, together with 3.6% yield of the isomer 6-fluoro-8-phenylsulfanyl-3,4-dihydro-2H-naphthalen-1-one: MP=111.7-112.7° C.; MS (M+1)=273; H1 NMR (300 MHz): δ(DMSO): 1.96 (2H, p, J=6.4 Hz), 2.53 (2H, t, J=6.03 Hz), 2.84 (2H, t, J=6.03 Hz), 6.69 (1H, dd, J=1.51, 12.06 Hz), 6.91 (1H, d, J=1.13 Hz), 7.5-7.61 (5H, m, Phenyl).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09365494B2
Quelldatensatzuspto-grants-2016_06
ORD IDord-79924d0183024a72b3e4ea9c4e36d57e
Quellennotizuspto-grants-2016_06