Ethyl chloroacetate → 1,2-Diethyl (1R,2R)-1,2-cyclopropanedicarboxylate

Ethyl-2-chloroacetate (147 g, 1.20 mol) was added to a stirred solution of ethyl prop-2-enoate (150 g, 1.50 mol) in DMF (700 mL) at 0° C. Sodium hydride (60% w/w, 48.0 g, 1.20 mol) was added portion-wise to the reaction mixture at 0° C. over a period of 2 hours. The reaction mixture was allowed to warm to room temperature. After 16 hours, the reaction mixture was quenched with ice water (500 mL) and extracted with ethyl acetate (2×1.0 L). The organic layers were combined, washed with water (500 mL) and then brine (500 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by chromatography on silica gel (10-20% ethyl acetate/petroleum ether, linear gradient) to afford diethyl rel-(1R,2R)-cyclopropane-1,2-dicarboxylate. 1H NMR (300 MHz, CDCl3) δ 4.20-4.10 (m, 4H), 2.10-2.05 (m, 2H), 1.48-1.40 (m, 2H), 1.35-1.20 (m, 6H).

1. customthe reaction mixture was quenched with ice water (500 mL)
2. extractionextracted with ethyl acetate (2×1.0 L)
3. washwashed with water (500 mL)
4. dry with materialbrine (500 mL), dried over anhydrous sodium sulfate
5. filtrationfiltered
6. concentrationconcentrated under reduced pressure
7. customThe residue was purified by chromatography on silica gel (10-20% ethyl acetate/petroleum ether, linear gradient)

ORD record

ord-fb0f794acf0549b690f461d924cb65a7

Source dataset

uspto-grants-2015_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09216173B2