Ethylene → 7-Bromo-2-tetralone

A solution of 3-bromophenylacetic acid (10.4 g, 48.4 mmol) in oxalyl chloride (50 mL, 0.57 mol) was stirred at ambient temperature for 5 min then at reflux for 5 h. The oxalyl chloride was removed in vacuo and the residue was dissolved in anhydrous CH2Cl2 (100 mL). This solution was added dropwise to a rapidly stirred, ice-cooled solution of AlCl3 (23.2 g, 174.2 mmol) in CH2Cl2 (500 mL). A stream of ethylene gas was blown into the vortex of the stirred solution during the addition and the reaction temperature was kept at <5° C. The reaction mixture was allowed to warm to ambient temperature and then poured onto ice and stirred vigorously. The organic portion was removed and the aqueous layer extracted with CH2Cl2 (2×200 mL). The combined CH2Cl2 fractions were passed through a 2″ pad of silica and concentrated to give a thick, red oil. The crude product was purified by silica gel chromatography, eluting with a gradient of hexane:EtOAc—100:0 to 75:25, to provide the title compound as a pale yellow solid. MS: m/z=226 (M+1).

1. temperatureat reflux for 5 h
2. customThe oxalyl chloride was removed in vacuo
3. dissolutionthe residue was dissolved in anhydrous CH2Cl2 (100 mL)
4. additionThis solution was added dropwise to
5. customwas kept at <5° C
6. additionpoured onto ice
7. stirringstirred vigorously
8. customThe organic portion was removed
9. extractionthe aqueous layer extracted with CH2Cl2 (2×200 mL)
10. concentrationconcentrated
11. customto give a thick, red oil
12. customThe crude product was purified by silica gel chromatography
13. washeluting with a gradient of hexane

ORD record

ord-a33107d2878c41b0a22ffdbeb3aff6d0

Source dataset

uspto-grants-2010_07

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07750010B2