2-Chloroethanol → HCID 21069785, compound

Temperature

60 °C

Zinc chloride (68.1 g, 0.5 mol) was fused under vacuum as described in the procedure for the synthesis of intermediate 1. The molten zinc was cooled and the evacuated flask was flushed with nitrogen. The flask was loaded with 2-ethyl-2-hydroxybutanenitrile, (40.3 g, 0.5 mol) and 2-chloroethanol (50.5 mL, 0.75 mmol) then stirred at 60° C. for 20 hours. The reaction mixture was diluted with water (250 mL) and extracted with dichloromethane (1×250 mL, 4×100 mL). The combined organic layers were dried (sodium sulfate), filtered, and concentrated in-vacuo. The crude product was purified by vacuum distillation (bp 83° C., 10 mmHg) to give the title compound (52 g). 1H NMR (500 MHz, CDCl3) δ ppm: 3.82 (2H, t, J=5.8 Hz), 3.64 (2H, t, J=5.8 Hz), 1.83 (4H, J=7.3 Hz), 1.03 (6H, t, J=7.6 Hz).

1. customthe evacuated flask was flushed with nitrogen
2. extractionextracted with dichloromethane (1×250 mL, 4×100 mL)
3. dry with materialThe combined organic layers were dried (sodium sulfate)
4. filtrationfiltered
5. concentrationconcentrated in-vacuo
6. distillationThe crude product was purified by vacuum distillation (bp 83° C., 10 mmHg)

ORD record

ord-097f951516c5402283480836bc5b7608

Source dataset

uspto-grants-2011_02

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07893055B2