Formaldehyde → Ethyl 2-propylacrylate

Temperature

23 °C

To a solution of ethyl n-propylmalonate (41.3 g, 237 mmol, 1 equiv) in EtOH (500 mL) at 23° C. was added piperidine (28.1 mL, 284 mmol, 1.2 equiv) followed by aqueous formaldehyde (37%, 88 mL). Following the addition, the reaction was refluxed for 29 h. After cooling to 23° C., the mixture was partitioned between diethyl ether (500 mL) and 1.0 N HCl (800 mL). The layers were separated and the aqueous layer was extracted with diethyl ether (500 mL). The combined organic layers were washed with H2O (500 mL), brine (300 mL), dried (MgSO4), filtered and concentrated (rotovap only, product is potentially volatile). The product was vacuum distilled (bp 70° C. at 15 mmHg) to give 16.4 g 21c (R9=n-propyl) (115 mmol, 49%) of the desired product: 1H NMR shows contamination with unidentified material; the product was used in the subsequent step without further purification: 1H NMR (300 MHz, CDCl3) 6.12 (s, 1H), 5.50 (s, 1H), 4.19 (q, J=7.2 Hz, 2H), 2.23 (t, J=7.5 Hz, 2H), 1.55–1.42 (m, 2H), 1.24 (t, J=7.2 Hz, 3H), 0.92 (t, J=7.5 Hz, 3H).

1. additionthe addition
2. temperaturethe reaction was refluxed for 29 h
3. customthe mixture was partitioned between diethyl ether (500 mL) and 1.0 N HCl (800 mL)
4. customThe layers were separated
5. extractionthe aqueous layer was extracted with diethyl ether (500 mL)
6. washThe combined organic layers were washed with H2O (500 mL), brine (300 mL)
7. dry with materialdried (MgSO4)
8. filtrationfiltered
9. concentrationconcentrated (rotovap only
10. distillationdistilled (bp 70° C. at 15 mmHg)

ORD record

ord-fb9556fea114435aa30a4c122f94e960

Source dataset

uspto-grants-2007_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07199106B2