Ethyl formate → 1-Cyclopropyl-3-(dimethylamino)prop-2-en-1-one

To a suspension of 5.94 g (0.11 mol) of sodium methoxide in 200 mL of dry THF was added 8.89 mL (0.11 mol) of ethyl formate, followed by methyl cyclopropyl ketone (9.91 mL, 0.10 mol, [765-43-5]). The reaction mixture rapidly turned yellow and was stirred at 25° for 4 hours. The reaction mixture was then concentrated and the residue was dissolved in 100 mL of methanol. To this was added a solution of 8.97 g (0.11 mol) of dimethylamine hydrochloride in 50 mL of methanol. The mixture was stirred for 1 hour at 25° , then the reaction mixture was concentrated. The residue was suspended in 100 mL of dry benzene and then concentrated. The residue was then triturated with 100 mL of dry benzene, filtered, and the filter cake was washed with additional dry benzene. The benzene solution was dried and concentrated to yield a yellow oil that crystallized upon cooling (11.97 g, 86%). mp 55°. NMR (CDCl3): 7.58 (d, 1 H); 5.21 (d, 1 H); 3.20-2.60 (br d, 6 H); 1.80 (m, 1 H); 1.00 (m, 2 H); 0.77 (m, 2 H). Mass spec 140 (M+H+).

1. concentrationThe reaction mixture was then concentrated
2. dissolutionthe residue was dissolved in 100 mL of methanol
3. stirringThe mixture was stirred for 1 hour at 25°
4. concentrationthe reaction mixture was concentrated
5. concentrationconcentrated
6. customThe residue was then triturated with 100 mL of dry benzene
7. filtrationfiltered
8. washthe filter cake was washed with additional dry benzene
9. dry with materialThe benzene solution was dried
10. concentrationconcentrated
11. customto yield a yellow oil
12. customthat crystallized
13. temperatureupon cooling (11.97 g, 86%)

ORDレコード

ord-175fe66eb4ac4d45b522a3b42d3dfdae

出典データセット

uspto-grants-1992_05

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US05110831