p-Toluenesulfonic acid → 1-(6-Methyl-pyrid-3-yl)-3,4-dihydro-4,4-dimethyl-7-bromo-naphthalene

To a cold (-78° C.) solution of 6-methyl-3-bromopyridine (890 mg, 5.2 mmol) in THF (15 mL) was added n-BuLi in hexane (1.6M solution, 3.5 mL, 5.6 mmol) and stirred for 1 hour. This mixture was added to a flask containing 3,4-dihydro-4,4-dimethyl-7-bromo-1(2H)-naphthalenone (Compound A, 1.35 g, 5.4 mmol), in THF (5 mL) at -78° C. The reaction mixture was gradually warmed to ambient temperature and stirred for 16 hours. Thereafter it was diluted with ethyl acetate (100 mL), washed with water (10 mL), brine (10 mL) and dried with MgSO4. Solvent was removed by distillation, the crude material was dissolved in toluene (25 mL) and pTSA (530 mg, 2.8 mmol) was added. The mixture was heated at 90° C. for 36 hours. Thereafter it was diluted with ethyl acetate (100 mL), washed with 10% NaHCO3 (2×10 mL), brine (10 mL), dried with MgSO4 and the solvent was removed by evaporation. The title compound was obtained by recrystallization from ethyl acetate and hexane mixture (1:9).

1. additionThis mixture was added to a flask
2. customat -78° C
3. stirringstirred for 16 hours
4. washwashed with water (10 mL), brine (10 mL)
5. dry with materialdried with MgSO4
6. customSolvent was removed by distillation
7. dissolutionthe crude material was dissolved in toluene (25 mL)
8. temperatureThe mixture was heated at 90° C. for 36 hours
9. washwashed with 10% NaHCO3 (2×10 mL), brine (10 mL)
10. dry with materialdried with MgSO4
11. customthe solvent was removed by evaporation

ORDレコード

ord-9920e201f1844369a4f53eaad2b0509b

出典データセット

uspto-grants-1998_03

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US05728846