反应详情

2-Acetylamino-6-methyl-6-nitroheptanoic acid (49.5 g, 200 mmol) was dissolved in water (246 ml) and 30% sodium hydroxide was added to adjust its pH to 8.87. L-Acylase (4.95 g) and anhydrous cobalt chloride (0.27 g) were added to adjust its pH to 9 and the mixture was stirred overnight at room temperature. Concentrated hydrochloric acid was added to adjust its pH to 1.5 and the mixture was ice-cooled. The precipitated crystals were separated by filtration and the filtrate was washed twice with a mixture (250 ml) of toluene-isopropyl alcohol (1:1) and the aqueous layer was concentrated under reduced pressure. Methanol (100 ml) was added for concentration and methanol (100 ml) was further added for concentration. As a result, the objective compound was obtained (20.5 g).

1. temperaturecooled
2. customThe precipitated crystals were separated by filtration
3. washthe filtrate was washed twice with a mixture (250 ml) of toluene-isopropyl alcohol (1:1)
4. concentrationthe aqueous layer was concentrated under reduced pressure
5. additionMethanol (100 ml) was added for concentration and methanol (100 ml)
6. additionwas further added for concentration
7. customAs a result, the objective compound was obtained (20.5 g)