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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262445Generated: November 1, 2026

Triethylamine → Isopropyl (2Z)-3-amino-2-cyano-4-ethyl-2-hexenoate

https://huagongshe.com/reaction/2262445

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantIsopropyl (2Z)-3-hydroxy-2-cyano-4-ethyl-2-hexenoateHCID 54693160—
SolventDichloromethaneHCID 6344—
ProductIsopropyl (2Z)-3-amino-2-cyano-4-ethyl-2-hexenoateHCID 11390469—

Reaction Conditions

Temperature0 °C

Reaction Steps

24.4 g (0.11 mol) of isopropyl (2Z)-3-hydroxy-2-cyano-4-ethyl-2-hexenoate were dissolved in CH2Cl2 and, at 25° C., 33.2 g (0.22 mol) of POCl3 were added. After cooling to 0° C., 43.8 g (0.44 mol) of triethylamine were added dropwise, and the mixture was stirred at 25° C. for 2 h. The solution was then concentrated and the residue was taken up in acetonitrile and cooled to 0° C., and 30 g (0.44 mol) of a 25 percent strength solution of ammonia were added dropwise. After 2 h of stirring, the mixture was concentrated to dryness, the residue was taken up in MTBE (methyl tert-butyl ether) and the organic phase was washed with NaOH and water, dried and concentrated. Purification by customary methods gave 10 g (40% of theory) of the title compound as a colorless solid (m.p. 140° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851411B2
Source datasetuspto-grants-2010_12
ORD IDord-1f3269e3fde34ad3a3eb295f921fe3db
Source noteuspto-grants-2010_12