Water → N-cyclopropylmethyl-3-bromopyrrolidine-2-one

In a 1.5-liter 4-necked flask, equipped with a stirrer, dropping funnel, reflux condenser, thermometer and argon inlet, 54.4 g sodium hydroxide pearls (1.36 mol) and 9.26 g tetrabutylammonium hydrogensulfate (27.3 mmol) were suspended with stirring at room temperature under argon in 500 ml dichloromethane. To the suspension 35.6 g aminomethylcyclopropane (500 mmol) were added. A solution of 100.0 g 2-bromo-4-chlorobutyric acid chloride (400 mmol, product of Example 1) in 100 ml dichloromethane was added during 10 min. After the first 3 min. of addition, reflux was reached and maintained during the addition. After completed addition, the mixture was refluxed for 1 h, during which its color changed from dark green to dark brown. The suspension was cooled to room temperature during 10 min., and a mixture of 50 g ice and 250 ml deionized water was added under stirring. The phases were separated and the organic layer was successively washed with a solution of 60 g ammonium chloride in 300 ml deionized water, followed by 300 ml deionized water. The organic layer was concentrated to yield 94.2 g of N-cyclopropylmethyl-3-bromopyrrolidine-2-one as a dark oil.

1. customIn a 1.5-liter 4-necked flask, equipped with a stirrer
2. temperaturereflux condenser
3. additionAfter the first 3 min. of addition
4. temperaturereflux
5. temperaturemaintained during the addition
6. additionaddition
7. temperaturethe mixture was refluxed for 1 h, during which its color
8. additionwas added
9. customThe phases were separated
10. washthe organic layer was successively washed with a solution of 60 g ammonium chloride in 300 ml
11. concentrationThe organic layer was concentrated

ORD record

ord-57f3a44f4fc34434829c92e433a08d3f

Source dataset

uspto-grants-2000_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06114541