Diisobutylaluminum hydride → HCID 59564912, compound

Temperature

-78 °C

DIBAL-H (73.6 mL, 110.4 mmol) (1.5M in Toluene) was added portionwise to a solution of tert-butyl 2,2-dimethyl-5-oxopyrrolidine-1-carboxylate (23.1 g, 108.3 mmol) in dry Et2O (200 mL) cooled to −78° C. The reaction was stirred for 1 hour at −78° C., allowed to warm to room temperature and stirred for 15 hours. The reaction was quenched with NH4OH (50 mL), stirred for 20 minutes, and then diluted with EtOAc (200 mL) and 0.5M Rochelle's Salt (100 mL). The layers were separated. The organic fraction was washed with 0.5M Rochelle's (2×100 mL), brine (100 mL), dried (MgSO4) and concentrated to an oil. The oil was taken up in a solution of p-TsOH monohydrate (2.0 g, 10.8 mmol) in MeOH (200 mL) and stirred for 15 hours at room temperature. The reaction was concentrated, taken up in EtOAc (200 mL), washed with saturated Na2CO3 (2×100 mL), brine (50 mL), dried (MgSO4) and concentrated to an oil, tert-butyl 5-methoxy-2,2-dimethylpyrrolidine-1-carboxylate (24.1 g, 97% yield).

1. temperatureto warm to room temperature
2. stirringstirred for 15 hours
3. customThe reaction was quenched with NH4OH (50 mL)
4. stirringstirred for 20 minutes
5. additiondiluted with EtOAc (200 mL) and 0.5M Rochelle's Salt (100 mL)
6. customThe layers were separated
7. washThe organic fraction was washed with 0.5M Rochelle's (2×100 mL), brine (100 mL)
8. dry with materialdried (MgSO4)
9. concentrationconcentrated to an oil
10. stirringstirred for 15 hours at room temperature
11. concentrationThe reaction was concentrated
12. washwashed with saturated Na2CO3 (2×100 mL), brine (50 mL)
13. dry with materialdried (MgSO4)

ORD record

ord-e7312667e5aa40678085076d330b54ca

Source dataset

uspto-grants-2013_02

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08372842B2