反应详情

N,N'-Carbonyldiimidazole (0.52 g) is added to a solution of 2-(2,6-dimethoxyphenyl)acetic acid (0.63 g) in dry dichloromethane (20 cc), cooled to +5° C. The mixture is stirred for 35 minutes at +5° C. The mixture is stirred for 35 minutes at +5° C. and a solution of (3aRS,7aRS)-7,7-diphenyl-4-perhydroisoindolone hydrochloride (1.05 g) and triethylamine (0.44 cc) in dichloromethane (25 cc) is then added. The reaction mixture is stirred at 20° C. for 16 hours, then washed with distilled water (2×50 cc), dried over magnesium sulphate and filtered and the filtrate is concentrated to dryness under reduced pressure (2.7 kPa). The residue is crystallized from a mixture of acetonitrile (16 cc) and isopropyl ether (15 cc). The crystals are drained, washed with isopropyl ether (10 cc) and dried. (3aRS,7aRS)-2-[(2,6-dimethoxyphenyl)acetyl]-7,7-diphenyl-4-perhydroisoindolone (0.89 g) melting at 224° C. is obtained.

1. temperaturecooled to +5° C
2. stirringThe mixture is stirred for 35 minutes at +5° C.
3. stirringThe reaction mixture is stirred at 20° C. for 16 hours
4. washwashed with distilled water (2×50 cc)
5. dry with materialdried over magnesium sulphate
6. filtrationfiltered
7. concentrationthe filtrate is concentrated to dryness under reduced pressure (2.7 kPa)
8. customThe residue is crystallized from a mixture of acetonitrile (16 cc) and isopropyl ether (15 cc)
9. washwashed with isopropyl ether (10 cc)
10. customdried