Formic Acid → 3-(1-Methylpyrrolidin-2-yl)pyridine

Temperatur

85 °C

To a solution of nornicotine (50 g 0.338 mol) in 100 ml water a mixture of 37% formaldehyde (49.7 g, 1.656 mol) and 85% formic acid (37.26 g 0.81 moles) was added and stirred at 85° C. for 20 hrs. The reaction was cooled and pH adjusted to >13 using NaOH, extracted with dichloromethane (100 ml×3) dried over Na2SO4 and solvent removed completely to get crude oil (52.5 g, 94.33% purity by GC). It was further purified by high vacuum distillation at 0.1 mm Hg to obtain colorless (R,S)-nicotine (44.54 g, 81.3% yield, 99.1% purity by GC). 1H NMR (CDCl3): δ 1.72-2.0 (3H, m), 2.1 (3H, s), 2.25 (1H, m), 2.3 (1H, m), 3.08 (1H, m), 3.23 (1 h, t), 7.25 (1H, m), 7.69 (1H, dt), and 8.5 (2H, m). 13C-NMR (CDCl3): 149.71, 148.76, 139, 134.97, 123.7, 68.9, 57.1, 40.5, 35.5, and 22.83. IR: 3233, 1642, and 1402 Cm−1.

1. additionwas added
2. temperatureThe reaction was cooled
3. extractionextracted with dichloromethane (100 ml×3)
4. dry with materialdried over Na2SO4 and solvent
5. customremoved completely
6. customto get crude oil (52.5 g, 94.33% purity by GC)
7. distillationIt was further purified by high vacuum distillation at 0.1 mm Hg

ORD-Eintrag

ord-2f0cdaa053cb4736b4a2d00846489562

Quelldatensatz

uspto-grants-2013_02

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08378110B1