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HRID 1246621Erstellt: 23. Oktober 2026

1,2-Dibromoethane → 2,3-Dihydro-1,4-benzoxathiin-6-ol

https://huagongshe.com/de/reaction/1246621

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DibromoethaneHCID 7839—
EduktPotassium CarbonateHCID 11430—
Edukt2-Mercaptobenzene-1,4-diolHCID 2736167—
LösungsmittelAcetoneHCID 180—
Produkt2,3-Dihydro-1,4-benzoxathiin-6-olHCID 1251591055,2%

Reaktionsschritte

1,2-Dibromoethane (2.3 mL, 26.7 mmol) and K2CO3 (8.21 g, 59.4 mmol) were slurried in acetone (250 mL) and a solution of 2-sulfanyl-1,4-benzenediol (prepared according to J. Org. Chem. 1990, 55, 2736) (4.22 g, 29.7 mmol) in acetone (50 mL) was added over 4 h to the stirred mixture. Once the addition was complete stirring was continued for a further 10 h before the solvent was removed in vacuo. The residue was partitioned between water (50 mL) and EtOAc (50 mL), the aqueous layer was extracted with EtOAc (50 mL) and the combined organic layers were dried (MgSO4) and evaporated. Purification of the residue by column chromatography [SiO2; 9:1 (pentane/EtOAc)] gave the title compound (2.48 g, 55%) as a pale orange oil; δH (CDCl3, 400 MHz) 3.08 (2H, m), 4.31 (2H, m), 4.44 (1H, s), 6.42 (1H, d), 6.49 (1H, s), 6.66 (1H, d); MS m/z (ES−) 167 (M−H+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07129234B2
Quelldatensatzuspto-grants-2006_10
ORD IDord-31422edad81740f2b974eb9bb032f709
Quellennotizuspto-grants-2006_10