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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Isopropyl (2Z)-3-hydroxy-2-cyano-4-ethyl-2-hexenoate | HCID 54693160 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Isopropyl (2Z)-3-amino-2-cyano-4-ethyl-2-hexenoate | HCID 11390469 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07851411B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-1f3269e3fde34ad3a3eb295f921fe3db |
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| Source note | uspto-grants-2010_12 |
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