反应详情

This material was made from 9,10 dibromoanthracene (Eastman, 20 g, 60 mmol) modifying the procedure of R. Kuhn and H. Fischer, Chem. Ber. 94 3060 (1961). In this procedure, the reaction mixture was cooled to -78° before the nBuLi was added. The resulting mixture was warmed to RT over 1 H and then refluxed until the crystalline starting material disappeared. The mixture was then cooled to -78° again before the DMF was added (in one portion). The flask was warmed to RT and then quenched with 1M HBr (200 mL). The two-phase system was then extracted with CH2Cl2 (3×500 mL). The extracts combined, dried (MgSO4), filtered, and the solvent removed to give the crude material. This was purified by preparative HPLC using PhCH3 as the eluting solvent. After the solvent was removed 13.06 g (76%) of 10-bromo-9-anthracenecarbaldehyde mp 215°-216.5°, lit. mp 218°, P. Kuhn and H. Fischer, Chem. Ber. 94 3060 (1961)), (C, H, Br) was obtained.

1. additionwas added
2. temperaturerefluxed until the
3. additionwas added (in one portion)
4. temperatureThe flask was warmed to RT
5. customquenched with 1M HBr (200 mL)
6. extractionThe two-phase system was then extracted with CH2Cl2 (3×500 mL)
7. dry with materialdried (MgSO4)
8. filtrationfiltered
9. customthe solvent removed
10. customto give the crude material
11. customThis was purified by preparative HPLC
12. customAfter the solvent was removed 13.06 g (76%) of 10-bromo-9-anthracenecarbaldehyde mp 215°-216.5°, lit. mp 218°, P
13. custom94 3060 (1961)), (C, H, Br) was obtained